A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated.
ARTHRITIS that is induced in experimental animals. Immunological methods and infectious agents can be used to develop experimental arthritis models. These methods include injections of stimulators of the immune response, such as an adjuvant (ADJUVANTS, IMMUNOLOGIC) or COLLAGEN.
Arthritis caused by BACTERIA; RICKETTSIA; MYCOPLASMA; VIRUSES; FUNGI; or PARASITES.
Arthritis of children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent.
A type of inflammatory arthritis associated with PSORIASIS, often involving the axial joints and the peripheral terminal interphalangeal joints. It is characterized by the presence of HLA-B27-associated SPONDYLARTHROPATHY, and the absence of rheumatoid factor.
An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN.
The inner membrane of a joint capsule surrounding a freely movable joint. It is loosely attached to the external fibrous capsule and secretes SYNOVIAL FLUID.
Also known as articulations, these are points of connection between the ends of certain separate bones, or where the borders of other bones are juxtaposed.
The clear, viscous fluid secreted by the SYNOVIAL MEMBRANE. It contains mucin, albumin, fat, and mineral salts and serves to lubricate joints.
Arthritis, especially of the great toe, as a result of gout. Acute gouty arthritis often is precipitated by trauma, infection, surgery, etc. The initial attacks are usually monoarticular but later attacks are often polyarticular.
Antibodies found in adult RHEUMATOID ARTHRITIS patients that are directed against GAMMA-CHAIN IMMUNOGLOBULINS.
Inflammation of a synovial membrane. It is usually painful, particularly on motion, and is characterized by a fluctuating swelling due to effusion within a synovial sac. (Dorland, 27th ed)
A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans.
A fibrillar collagen found predominantly in CARTILAGE and vitreous humor. It consists of three identical alpha1(II) chains.
An antineoplastic antimetabolite with immunosuppressant properties. It is an inhibitor of TETRAHYDROFOLATE DEHYDROGENASE and prevents the formation of tetrahydrofolate, necessary for synthesis of thymidylate, an essential component of DNA.
Levels within a diagnostic group which are established by various measurement criteria applied to the seriousness of a patient's disorder.
Antibodies that react with self-antigens (AUTOANTIGENS) of the organism that produced them.
Measurement of rate of settling of erythrocytes in anticoagulated blood.
Methods of delivering drugs into a joint space.
Serum glycoprotein produced by activated MACROPHAGES and other mammalian MONONUCLEAR LEUKOCYTES. It has necrotizing activity against tumor cell lines and increases ability to reject tumor transplants. Also known as TNF-alpha, it is only 30% homologous to TNF-beta (LYMPHOTOXIN), but they share TNF RECEPTORS.
Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement.
The major immunoglobulin isotype class in normal human serum. There are several isotype subclasses of IgG, for example, IgG1, IgG2A, and IgG2B.
Roentgenography of a joint, usually after injection of either positive or negative contrast medium.
A subspecialty of internal medicine concerned with the study of inflammatory or degenerative processes and metabolic derangement of connective tissue structures which pertain to a variety of musculoskeletal disorders, such as arthritis.
A synovial hinge connection formed between the bones of the FEMUR; TIBIA; and PATELLA.
The articulation between a metacarpal bone and a phalanx.
A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions.
A drug that is used in the management of inflammatory bowel diseases. Its activity is generally considered to lie in its metabolic breakdown product, 5-aminosalicylic acid (see MESALAMINE) released in the colon. (From Martindale, The Extra Pharmacopoeia, 30th ed, p907)
Peptides whose amino and carboxy ends are linked together with a peptide bond forming a circular chain. Some of them are ANTI-INFECTIVE AGENTS. Some of them are biosynthesized non-ribosomally (PEPTIDE BIOSYNTHESIS, NON-RIBOSOMAL).
Disorders that are characterized by the production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides.
Antibodies produced by a single clone of cells.
A variable mixture of the mono- and disodium salts of gold thiomalic acid used mainly for its anti-inflammatory action in the treatment of rheumatoid arthritis. It is most effective in active progressive rheumatoid arthritis and of little or no value in the presence of extensive deformities or in the treatment of other forms of arthritis.
The joint that is formed by the distal end of the RADIUS, the articular disc of the distal radioulnar joint, and the proximal row of CARPAL BONES; (SCAPHOID BONE; LUNATE BONE; triquetral bone).
Subcutaneous nodules seen in 20-30% of rheumatoid arthritis patients. They may arise anywhere on the body, but are most frequently found over the bony prominences. The nodules are characterized histologically by dense areas of fibrinoid necrosis with basophilic streaks and granules, surrounded by a palisade of cells, mainly fibroblasts and histiocytes.
A polypeptide substance comprising about one third of the total protein in mammalian organisms. It is the main constituent of SKIN; CONNECTIVE TISSUE; and the organic substance of bones (BONE AND BONES) and teeth (TOOTH).
A subtype of HLA-DRB beta chains that includes over one hundred allele variants. The HLA-DRB1 subtype is associated with several of the HLA-DR SEROLOGICAL SUBTYPES.
The articulation between the head of one phalanx and the base of the one distal to it, in each finger.
Naturally occurring or experimentally induced animal diseases with pathological processes sufficiently similar to those of human diseases. They are used as study models for human diseases.
Evaluation undertaken to assess the results or consequences of management and procedures used in combating disease in order to determine the efficacy, effectiveness, safety, and practicability of these interventions in individual cases or series.
The articulations between the various TARSAL BONES. This does not include the ANKLE JOINT which consists of the articulations between the TIBIA; FIBULA; and TALUS.
An infectious disease caused by a spirochete, BORRELIA BURGDORFERI, which is transmitted chiefly by Ixodes dammini (see IXODES) and pacificus ticks in the United States and Ixodes ricinis (see IXODES) in Europe. It is a disease with early and late cutaneous manifestations plus involvement of the nervous system, heart, eye, and joints in variable combinations. The disease was formerly known as Lyme arthritis and first discovered at Old Lyme, Connecticut.
Cell surface receptors that bind TUMOR NECROSIS FACTORS and trigger changes which influence the behavior of cells.
An HLA-DR antigen which is associated with HLA-DRB1 CHAINS encoded by DRB1*04 alleles.
Substances that reduce or suppress INFLAMMATION.
A subclass of HLA-D antigens that consist of alpha and beta chains. The inheritance of HLA-DR antigens differs from that of the HLA-DQ ANTIGENS and HLA-DP ANTIGENS.
Non-antibody proteins secreted by inflammatory leukocytes and some non-leukocytic cells, that act as intercellular mediators. They differ from classical hormones in that they are produced by a number of tissue or cell types rather than by specialized glands. They generally act locally in a paracrine or autocrine rather than endocrine manner.
Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others.
The articulations extending from the ANKLE distally to the TOES. These include the ANKLE JOINT; TARSAL JOINTS; METATARSOPHALANGEAL JOINT; and TOE JOINT.
A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis.
A protective layer of firm, flexible cartilage over the articulating ends of bones. It provides a smooth surface for joint movement, protecting the ends of long bones from wear at points of contact.
The joint that is formed by the inferior articular and malleolar articular surfaces of the TIBIA; the malleolar articular surface of the FIBULA; and the medial malleolar, lateral malleolar, and superior surfaces of the TALUS.
A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function.
Lymphocytes responsible for cell-mediated immunity. Two types have been identified - cytotoxic (T-LYMPHOCYTES, CYTOTOXIC) and helper T-lymphocytes (T-LYMPHOCYTES, HELPER-INDUCER). They are formed when lymphocytes circulate through the THYMUS GLAND and differentiate to thymocytes. When exposed to an antigen, they divide rapidly and produce large numbers of new T cells sensitized to that antigen.
A proinflammatory cytokine produced primarily by T-LYMPHOCYTES or their precursors. Several subtypes of interleukin-17 have been identified, each of which is a product of a unique gene.
Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE.
An antigen solution emulsified in mineral oil. The complete form is made up of killed, dried mycobacteria, usually M. tuberculosis, suspended in the oil phase. It is effective in stimulating cell-mediated immunity (IMMUNITY, CELLULAR) and potentiates the production of certain IMMUNOGLOBULINS in some animals. The incomplete form does not contain mycobacteria.
The region in the hindlimb of a quadruped, corresponding to the human ANKLE.
An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed.
Inflammation of the synovial lining of a tendon sheath. Causes include trauma, tendon stress, bacterial disease (gonorrhea, tuberculosis), rheumatic disease, and gout. Common sites are the hand, wrist, shoulder capsule, hip capsule, hamstring muscles, and Achilles tendon. The tendon sheaths become inflamed and painful, and accumulate fluid. Joint mobility is usually reduced.
A specific HLA-B surface antigen subtype. Members of this subtype contain alpha chains that are encoded by the HLA-B*27 allele family.
Measurable and quantifiable biological parameters (e.g., specific enzyme concentration, specific hormone concentration, specific gene phenotype distribution in a population, presence of biological substances) which serve as indices for health- and physiology-related assessments, such as disease risk, psychiatric disorders, environmental exposure and its effects, disease diagnosis, metabolic processes, substance abuse, pregnancy, cell line development, epidemiologic studies, etc.
Organic compounds that contain GOLD as an integral part of the molecule. Some are used as ANTIRHEUMATIC AGENTS. The term chrysotherapy derives from an ancient Greek term for gold.
Therapy with two or more separate preparations given for a combined effect.
The articulations extending from the WRIST distally to the FINGERS. These include the WRIST JOINT; CARPAL JOINTS; METACARPOPHALANGEAL JOINT; and FINGER JOINT.
An aldose-ketose isomerase that catalyzes the reversible interconversion of glucose 6-phosphate and fructose 6-phosphate. In prokaryotic and eukaryotic organisms it plays an essential role in glycolytic and gluconeogenic pathways. In mammalian systems the enzyme is found in the cytoplasm and as a secreted protein. This secreted form of glucose-6-phosphate isomerase has been referred to as autocrine motility factor or neuroleukin, and acts as a cytokine which binds to the AUTOCRINE MOTILITY FACTOR RECEPTOR. Deficiency of the enzyme in humans is an autosomal recessive trait, which results in CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA.
Determination of the degree of a physical, mental, or emotional handicap. The diagnosis is applied to legal qualification for benefits and income under disability insurance and to eligibility for Social Security and workmen's compensation benefits.
An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS.
A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow.
Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others.
A cytokine that stimulates the growth and differentiation of B-LYMPHOCYTES and is also a growth factor for HYBRIDOMAS and plasmacytomas. It is produced by many different cells including T-LYMPHOCYTES; MONOCYTES; and FIBROBLASTS.
Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care. (Dictionary of Health Services Management, 2d ed)
A soluble factor produced by MONOCYTES; MACROPHAGES, and other cells which activates T-lymphocytes and potentiates their response to mitogens or antigens. Interleukin-1 is a general term refers to either of the two distinct proteins, INTERLEUKIN-1ALPHA and INTERLEUKIN-1BETA. The biological effects of IL-1 include the ability to replace macrophage requirements for T-cell activation.
A latent susceptibility to disease at the genetic level, which may be activated under certain conditions.
A ligand that binds to but fails to activate the INTERLEUKIN 1 RECEPTOR. It plays an inhibitory role in the regulation of INFLAMMATION and FEVER. Several isoforms of the protein exist due to multiple ALTERNATIVE SPLICING of its mRNA.
A non-vascular form of connective tissue composed of CHONDROCYTES embedded in a matrix that includes CHONDROITIN SULFATE and various types of FIBRILLAR COLLAGEN. There are three major types: HYALINE CARTILAGE; FIBROCARTILAGE; and ELASTIC CARTILAGE.
Component of the NATIONAL INSTITUTES OF HEALTH. It supports research into the causes, treatment, and prevention of arthritis and musculoskeletal and skin diseases; the training of basic and clinical scientists to carry out this research; and the dissemination of information on research progress. It was established in 1986.
Elements of limited time intervals, contributing to particular results or situations.
Studies which start with the identification of persons with a disease of interest and a control (comparison, referent) group without the disease. The relationship of an attribute to the disease is examined by comparing diseased and non-diseased persons with regard to the frequency or levels of the attribute in each group.
Azoles with an OXYGEN and a NITROGEN next to each other at the 1,2 positions, in contrast to OXAZOLES that have nitrogens at the 1,3 positions.
Endogenous tissue constituents that have the ability to interact with AUTOANTIBODIES and cause an immune response.
A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states.
3-Mercapto-D-valine. The most characteristic degradation product of the penicillin antibiotics. It is used as an antirheumatic and as a chelating agent in Wilson's disease.
A specific species of bacteria, part of the BORRELIA BURGDORFERI GROUP, whose common name is Lyme disease spirochete.
A class of immunoglobulin bearing mu chains (IMMUNOGLOBULIN MU-CHAINS). IgM can fix COMPLEMENT. The name comes from its high molecular weight and originally being called a macroglobulin.
Either of two extremities of four-footed non-primate land animals. It usually consists of a FEMUR; TIBIA; and FIBULA; tarsals; METATARSALS; and TOES. (From Storer et al., General Zoology, 6th ed, p73)
Infections with bacteria of the genus YERSINIA.
Pain in the joint.
Inflammation of the joints of the SPINE, the intervertebral articulations.
Process whereby the immune system reacts against the body's own tissues. Autoimmunity may produce or be caused by AUTOIMMUNE DISEASES.
Scales, questionnaires, tests, and other methods used to assess pain severity and duration in patients or experimental animals to aid in diagnosis, therapy, and physiological studies.
The articulation between the head of one phalanx and the base of the one distal to it, in each toe.
Studies in which individuals or populations are followed to assess the outcome of exposures, procedures, or effects of a characteristic, e.g., occurrence of disease.
Connective tissue cells which secrete an extracellular matrix rich in collagen and other macromolecules.
A large multinuclear cell associated with the BONE RESORPTION. An odontoclast, also called cementoclast, is cytomorphologically the same as an osteoclast and is involved in CEMENTUM resorption.
A group of CORTICOSTEROIDS that affect carbohydrate metabolism (GLUCONEOGENESIS, liver glycogen deposition, elevation of BLOOD SUGAR), inhibit ADRENOCORTICOTROPIC HORMONE secretion, and possess pronounced anti-inflammatory activity. They also play a role in fat and protein metabolism, maintenance of arterial blood pressure, alteration of the connective tissue response to injury, reduction in the number of circulating lymphocytes, and functioning of the central nervous system.
Autoantibodies directed against various nuclear antigens including DNA, RNA, histones, acidic nuclear proteins, or complexes of these molecular elements. Antinuclear antibodies are found in systemic autoimmune diseases including systemic lupus erythematosus, Sjogren's syndrome, scleroderma, polymyositis, and mixed connective tissue disease.
The complex formed by the binding of antigen and antibody molecules. The deposition of large antigen-antibody complexes leading to tissue damage causes IMMUNE COMPLEX DISEASES.
A plasma protein that circulates in increased amounts during inflammation and after tissue damage.
Deformities of the hand, or a part of the hand, acquired after birth as the result of injury or disease.
Strains of mice in which certain GENES of their GENOMES have been disrupted, or "knocked-out". To produce knockouts, using RECOMBINANT DNA technology, the normal DNA sequence of the gene being studied is altered to prevent synthesis of a normal gene product. Cloned cells in which this DNA alteration is successful are then injected into mouse EMBRYOS to produce chimeric mice. The chimeric mice are then bred to yield a strain in which all the cells of the mouse contain the disrupted gene. Knockout mice are used as EXPERIMENTAL ANIMAL MODELS for diseases (DISEASE MODELS, ANIMAL) and to clarify the functions of the genes.
Antibodies from non-human species whose protein sequences have been modified to make them nearly identical with human antibodies. If the constant region and part of the variable region are replaced, they are called humanized. If only the constant region is modified they are called chimeric. INN names for humanized antibodies end in -zumab.
Morphologic alteration of small B LYMPHOCYTES or T LYMPHOCYTES in culture into large blast-like cells able to synthesize DNA and RNA and to divide mitotically. It is induced by INTERLEUKINS; MITOGENS such as PHYTOHEMAGGLUTININS, and by specific ANTIGENS. It may also occur in vivo as in GRAFT REJECTION.
Immunoglobulin molecules having a specific amino acid sequence by virtue of which they interact only with the ANTIGEN (or a very similar shape) that induced their synthesis in cells of the lymphoid series (especially PLASMA CELLS).
Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-CELLS or by inhibiting the activation of HELPER CELLS. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of INTERLEUKINS and other CYTOKINES are emerging.
Studies in which subsets of a defined population are identified. These groups may or may not be exposed to factors hypothesized to influence the probability of the occurrence of a particular disease or other outcome. Cohorts are defined populations which, as a whole, are followed in an attempt to determine distinguishing subgroup characteristics.
Bone loss due to osteoclastic activity.
An extracellular endopeptidase of vertebrate tissues similar to MATRIX METALLOPROTEINASE 1. It digests PROTEOGLYCAN; FIBRONECTIN; COLLAGEN types III, IV, V, and IX, and activates procollagenase. (Enzyme Nomenclature, 1992)
An interleukin-1 subtype that is synthesized as an inactive membrane-bound pro-protein. Proteolytic processing of the precursor form by CASPASE 1 results in release of the active form of interleukin-1beta from the membrane.
Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group.
A rare complication of rheumatoid arthritis with autoimmune NEUTROPENIA; and SPLENOMEGALY.
The distal extremity of the leg in vertebrates, consisting of the tarsus (ANKLE); METATARSUS; phalanges; and the soft tissues surrounding these bones.
A method of studying a drug or procedure in which both the subjects and investigators are kept unaware of who is actually getting which specific treatment.
The distal part of the arm beyond the wrist in humans and primates, that includes the palm, fingers, and thumb.
Lymphoid cells concerned with humoral immunity. They are short-lived cells resembling bursa-derived lymphocytes of birds in their production of immunoglobulin upon appropriate stimulation.
A double gliding joint formed by the CLAVICLE, superior and lateral parts of the manubrium sterni at the clavicular notch, and the cartilage of the first rib.
The endogenous compounds that mediate inflammation (AUTACOIDS) and related exogenous compounds including the synthetic prostaglandins (PROSTAGLANDINS, SYNTHETIC).
The articulation between a metatarsal bone (METATARSAL BONES) and a phalanx.
An oral chrysotherapeutic agent for the treatment of rheumatoid arthritis. Its exact mechanism of action is unknown, but it is believed to act via immunological mechanisms and alteration of lysosomal enzyme activity. Its efficacy is slightly less than that of injected gold salts, but it is better tolerated, and side effects which occur are potentially less serious.
Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis.
The relatively long-lived phagocytic cell of mammalian tissues that are derived from blood MONOCYTES. Main types are PERITONEAL MACROPHAGES; ALVEOLAR MACROPHAGES; HISTIOCYTES; KUPFFER CELLS of the liver; and OSTEOCLASTS. They may further differentiate within chronic inflammatory lesions to EPITHELIOID CELLS or may fuse to form FOREIGN BODY GIANT CELLS or LANGHANS GIANT CELLS. (from The Dictionary of Cell Biology, Lackie and Dow, 3rd ed.)
A specialized CONNECTIVE TISSUE that is the main constituent of the SKELETON. The principle cellular component of bone is comprised of OSTEOBLASTS; OSTEOCYTES; and OSTEOCLASTS, while FIBRILLAR COLLAGENS and hydroxyapatite crystals form the BONE MATRIX.
A subtype of non-receptor protein tyrosine phosphatases that is characterized by the presence of an N-terminal catalytic domain and a C-terminal PROLINE-rich domain. The phosphatase subtype is predominantly expressed in LYMPHOCYTES and plays a key role in the inhibition of downstream T-LYMPHOCYTE activation. Polymorphisms in the gene that encodes this phosphatase subtype are associated with a variety of AUTOIMMUNE DISEASES.
Hereditary metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with formation of uric acid calculi.
The major interferon produced by mitogenically or antigenically stimulated LYMPHOCYTES. It is structurally different from TYPE I INTERFERON and its major activity is immunoregulation. It has been implicated in the expression of CLASS II HISTOCOMPATIBILITY ANTIGENS in cells that do not normally produce them, leading to AUTOIMMUNE DISEASES.
Inflammation of the SPINE. This includes both arthritic and non-arthritic conditions.
Inflammation of the bone.
A species of LENTIVIRUS, subgenus ovine-caprine lentiviruses (LENTIVIRUSES, OVINE-CAPRINE), closely related to VISNA-MAEDI VIRUS and causing acute encephalomyelitis; chronic arthritis; PNEUMONIA; MASTITIS; and GLOMERULONEPHRITIS in goats. It is transmitted mainly in the colostrum and milk.
Treatment of diseases with biological materials or biological response modifiers, such as the use of GENES; CELLS; TISSUES; organs; SERUM; VACCINES; and humoral agents.
Complex pharmaceutical substances, preparations, or matter derived from organisms usually obtained by biological methods or assay.
A class of statistical methods applicable to a large set of probability distributions used to test for correlation, location, independence, etc. In most nonparametric statistical tests, the original scores or observations are replaced by another variable containing less information. An important class of nonparametric tests employs the ordinal properties of the data. Another class of tests uses information about whether an observation is above or below some fixed value such as the median, and a third class is based on the frequency of the occurrence of runs in the data. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1284; Corsini, Concise Encyclopedia of Psychology, 1987, p764-5)
A transmembrane protein belonging to the tumor necrosis factor superfamily that specifically binds RECEPTOR ACTIVATOR OF NUCLEAR FACTOR-KAPPA B and OSTEOPROTEGERIN. It plays an important role in regulating OSTEOCLAST differentiation and activation.
The level of health of the individual, group, or population as subjectively assessed by the individual or by more objective measures.
Sites on an antigen that interact with specific antibodies.
Laboratory mice that have been produced from a genetically manipulated EGG or EMBRYO, MAMMALIAN.
Granular leukocytes having a nucleus with three to five lobes connected by slender threads of chromatin, and cytoplasm containing fine inconspicuous granules and stainable by neutral dyes.
Technique using an instrument system for making, processing, and displaying one or more measurements on individual cells obtained from a cell suspension. Cells are usually stained with one or more fluorescent dyes specific to cell components of interest, e.g., DNA, and fluorescence of each cell is measured as it rapidly transverses the excitation beam (laser or mercury arc lamp). Fluorescence provides a quantitative measure of various biochemical and biophysical properties of the cell, as well as a basis for cell sorting. Other measurable optical parameters include light absorption and light scattering, the latter being applicable to the measurement of cell size, shape, density, granularity, and stain uptake.
The genetic constitution of the individual, comprising the ALLELES present at each GENETIC LOCUS.
RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm.
Methods to determine in patients the nature of a disease or disorder at its early stage of progression. Generally, early diagnosis improves PROGNOSIS and TREATMENT OUTCOME.
Predetermined sets of questions used to collect data - clinical data, social status, occupational group, etc. The term is often applied to a self-completed survey instrument.
An aspect of personal behavior or lifestyle, environmental exposure, or inborn or inherited characteristic, which, on the basis of epidemiologic evidence, is known to be associated with a health-related condition considered important to prevent.
Subset of helper-effector T-lymphocytes which synthesize and secrete IL-17, IL-17F, and IL-22. These cytokines are involved in host defenses and tissue inflammation in autoimmune diseases.
The performance of the basic activities of self care, such as dressing, ambulation, or eating.
A thioglucose derivative used as an antirheumatic and experimentally to produce obesity in animals.
Diseases of BONES.
A constitution or condition of the body which makes the tissues react in special ways to certain extrinsic stimuli and thus tends to make the individual more than usually susceptible to certain diseases.
Gram-negative helical bacteria, in the genus BORRELIA, that are the etiologic agents of LYME DISEASE. The group comprises many specific species including Borrelia afzelii, Borellia garinii, and BORRELIA BURGDORFERI proper. These spirochetes are generally transmitted by several species of ixodid ticks.
Glycoproteins which contain sialic acid as one of their carbohydrates. They are often found on or in the cell or tissue membranes and participate in a variety of biological activities.
Glycoproteins which have a very high polysaccharide content.
An encapsulated lymphatic organ through which venous blood filters.
The surgical fixation of a joint by a procedure designed to accomplish fusion of the joint surfaces by promoting the proliferation of bone cells. (Dorland, 28th ed)
The distance and direction to which a bone joint can be extended. Range of motion is a function of the condition of the joints, muscles, and connective tissues involved. Joint flexibility can be improved through appropriate MUSCLE STRETCHING EXERCISES.
Partial or total replacement of a joint.
A critical subpopulation of T-lymphocytes involved in the induction of most immunological functions. The HIV virus has selective tropism for the T4 cell which expresses the CD4 phenotypic marker, a receptor for HIV. In fact, the key element in the profound immunosuppression seen in HIV infection is the depletion of this subset of T-lymphocytes.
Biologically active substances whose activities affect or play a role in the functioning of the immune system.
Combinations of diagnostic or therapeutic substances linked with specific immune substances such as IMMUNOGLOBULINS; MONOCLONAL ANTIBODIES; or ANTIGENS. Often the diagnostic or therapeutic substance is a radionuclide. These conjugates are useful tools for specific targeting of DRUGS and RADIOISOTOPES in the CHEMOTHERAPY and RADIOIMMUNOTHERAPY of certain cancers.
Prostheses used to partially or totally replace a human or animal joint. (from UMDNS, 1999)
Large, phagocytic mononuclear leukocytes produced in the vertebrate BONE MARROW and released into the BLOOD; contain a large, oval or somewhat indented nucleus surrounded by voluminous cytoplasm and numerous organelles.
Variant forms of the same gene, occupying the same locus on homologous CHROMOSOMES, and governing the variants in production of the same gene product.
In horses, cattle, and other quadrupeds, the joint between the femur and the tibia, corresponding to the human knee.
Surgical reconstruction of a joint to relieve pain or restore motion.
Noninflammatory degenerative disease of the knee joint consisting of three large categories: conditions that block normal synchronous movement, conditions that produce abnormal pathways of motion, and conditions that cause stress concentration resulting in changes to articular cartilage. (Crenshaw, Campbell's Operative Orthopaedics, 8th ed, p2019)
Tuberculosis of the bones or joints.
A variation of the PCR technique in which cDNA is made from RNA via reverse transcription. The resultant cDNA is then amplified using standard PCR protocols.
The relationship between the dose of an administered drug and the response of the organism to the drug.
Studies used to test etiologic hypotheses in which inferences about an exposure to putative causal factors are derived from data relating to characteristics of persons under study or to events or experiences in their past. The essential feature is that some of the persons under study have the disease or outcome of interest and their characteristics are compared with those of unaffected persons.
Distortion or disfigurement of the foot, or a part of the foot, acquired through disease or injury after birth.
The production of ANTIBODIES by proliferating and differentiated B-LYMPHOCYTES under stimulation by ANTIGENS.
A hinge joint connecting the FOREARM to the ARM.
A cytokine produced by a variety of cell types, including T-LYMPHOCYTES; MONOCYTES; DENDRITIC CELLS; and EPITHELIAL CELLS that exerts a variety of effects on immunoregulation and INFLAMMATION. Interleukin-10 combines with itself to form a homodimeric molecule that is the biologically active form of the protein.
The total number of cases of a given disease in a specified population at a designated time. It is differentiated from INCIDENCE, which refers to the number of new cases in the population at a given time.
Specific molecular sites on the surface of various cells, including B-lymphocytes and macrophages, that combine with IMMUNOGLOBULIN Gs. Three subclasses exist: Fc gamma RI (the CD64 antigen, a low affinity receptor), Fc gamma RII (the CD32 antigen, a high affinity receptor), and Fc gamma RIII (the CD16 antigen, a low affinity receptor).
Serum albumin from cows, commonly used in in vitro biological studies. (From Stedman, 25th ed)
The joint involving the CERVICAL ATLAS and axis bones.
PROTEOGLYCANS-associated proteins that are major components of EXTRACELLULAR MATRIX of various tissues including CARTILAGE; and INTERVERTEBRAL DISC structures. They bind COLLAGEN fibers and contain protein domains that enable oligomer formation and interaction with other extracellular matrix proteins such as CARTILAGE OLIGOMERIC MATRIX PROTEIN.
The joint that is formed by the articulation of the head of FEMUR and the ACETABULUM of the PELVIS.
A generic concept reflecting concern with the modification and enhancement of life attributes, e.g., physical, political, moral and social environment; the overall condition of a human life.
Antibodies which react with the individual structural determinants (idiotopes) on the variable region of other antibodies.
The age, developmental stage, or period of life at which a disease or the initial symptoms or manifestations of a disease appear in an individual.
A single nucleotide variation in a genetic sequence that occurs at appreciable frequency in the population.
Antigens determined by leukocyte loci found on chromosome 6, the major histocompatibility loci in humans. They are polypeptides or glycoproteins found on most nucleated cells and platelets, determine tissue types for transplantation, and are associated with certain diseases.
Histochemical localization of immunoreactive substances using labeled antibodies as reagents.
The phenotypic manifestation of a gene or genes by the processes of GENETIC TRANSCRIPTION and GENETIC TRANSLATION.
Endoscopic examination, therapy and surgery of the joint.
Presence of calcium salts, especially calcium pyrophosphate, in the cartilaginous structures of one or more joints. When accompanied by attacks of goutlike symptoms, it is called pseudogout. (Dorland, 27th ed)
A family of zinc-dependent metalloendopeptidases that is involved in the degradation of EXTRACELLULAR MATRIX components.
A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides.
Mature LYMPHOCYTES and MONOCYTES transported by the blood to the body's extravascular space. They are morphologically distinguishable from mature granulocytic leukocytes by their large, non-lobed nuclei and lack of coarse, heavily stained cytoplasmic granules.
The immovable joint formed by the lateral surfaces of the SACRUM and ILIUM.
The CARPAL BONES; METACARPAL BONES; and FINGER PHALANGES. In each hand there are eight carpal bones, five metacarpal bones, and 14 phalanges.
A class of compounds composed of repeating 5-carbon units of HEMITERPENES.
Large HYALURONAN-containing proteoglycans found in articular cartilage (CARTILAGE, ARTICULAR). They form into aggregates that provide tissues with the capacity to resist high compressive and tensile forces.
The statistical reproducibility of measurements (often in a clinical context), including the testing of instrumentation or techniques to obtain reproducible results. The concept includes reproducibility of physiological measurements, which may be used to develop rules to assess probability or prognosis, or response to a stimulus; reproducibility of occurrence of a condition; and reproducibility of experimental results.
A fluid-filled sac lined with SYNOVIAL MEMBRANE that provides a cushion between bones, tendons and/or muscles around a joint.
Disease having a short and relatively severe course.

Association of the inflammatory state in active juvenile rheumatoid arthritis with hypo-high-density lipoproteinemia and reduced lipoprotein-associated platelet-activating factor acetylhydrolase activity. (1/962)

OBJECTIVE: To investigate the relationship between the quantitative and qualitative abnormalities of apolipoprotein B (Apo B)- and Apo A-I-containing lipoproteins and between lipoprotein-associated platelet-activating factor acetylhydrolase (PAF-AH) activity in patients with juvenile rheumatoid arthritis (JRA) as a function of the inflammatory state. METHODS: Twenty-six JRA patients and 22 age- and sex-matched control subjects with normal lipid levels participated in the study. Fourteen patients had active disease, and 12 had inactive disease. Plasma lipoproteins were fractionated by gradient ultracentrifugation into 9 subfractions, and their chemical composition and mass were determined. The PAF-AH activity associated with lipoprotein subfractions and the activity in plasma were also measured. RESULTS: Patients with active JRA had significantly lower plasma total cholesterol and high-density lipoprotein (HDL) cholesterol levels as compared with controls, due to the decrease in the mass of both the HDL2 and HDL3 subfractions. Patients with active JRA also had higher plasma triglyceride levels, mainly due to the higher triglyceride content of the very low-density lipoprotein plus the intermediate-density lipoprotein subfraction. The plasma PAF-AH activity in patients with active JRA was lower than that in controls, mainly due to the decrease in PAF-AH activity associated with the intermediate and dense low-density lipoprotein subclasses. The lipid abnormalities and the reduction in plasma PAF-AH activity were significantly correlated with plasma C-reactive protein levels and were not observed in patients with inactive JRA. CONCLUSION: This is the first study to show that patients with active JRA exhibit low levels of HDL2 and HDL3 and are deficient in plasma PAF-AH activity. These alterations suggest that active JRA is associated with partial loss of the antiinflammatory activity of plasma Apo B- and Apo A-I-containing lipoproteins.  (+info)

Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease associations. (2/962)

The frequent variations of human complement component C4 gene size and gene numbers, plus the extensive polymorphism of the proteins, render C4 an excellent marker for major histocompatibility complex disease associations. As shown by definitive RFLPs, the tandemly arranged genes RP, C4, CYP21, and TNX are duplicated together as a discrete genetic unit termed the RCCX module. Duplications of the RCCX modules occurred by the addition of genomic fragments containing a long (L) or a short (S) C4 gene, a CYP21A or a CYP21B gene, and the gene fragments TNXA and RP2. Four major RCCX structures with bimodular L-L, bimodular L-S, monomodular L, and monomodular S are present in the Caucasian population. These modules are readily detectable by TaqI RFLPs. The RCCX modular variations appear to be a root cause for the acquisition of deleterious mutations from pseudogenes or gene segments in the RCCX to their corresponding functional genes. In a patient with congenital adrenal hyperplasia, we discovered a TNXB-TNXA recombinant with the deletion of RP2-C4B-CYP21B. Elucidation of the DNA sequence for the recombination breakpoint region and sequence analyses yielded definitive proof for an unequal crossover between TNXA from a bimodular chromosome and TNXB from a monomodular chromosome.  (+info)

Assessment of bone mineral density in adults with a history of juvenile chronic arthritis: a cross-sectional long-term followup study. (3/962)

OBJECTIVE: To assess bone mineral density (BMD) and bone turnover in adults with a history of juvenile chronic arthritis (JCA) or persistent JCA, and to identify predictors of reduced BMD. METHODS: Sixty-five white patients (mean age 32.2 years) with a history of JCA and 65 age-, sex-, height-, and weight-matched healthy control subjects participated in the study. Densitometry of the left hip and the lumbar spine was performed, and osteocalcin (bone formation marker) and crosslinks (bone resorption marker) were measured. In addition, bone-related clinical parameters were assessed in the JCA group. RESULTS: BMD in the hip and lumbar spine was significantly lower in the JCA group than in the controls. Levels of osteocalcin and crosslinks were significantly increased in the JCA group. According to WHO definitions, significantly more subjects in the JCA group had "osteopenia" and "osteoporosis" than would be expected in a normal population sample. Active disease at the time of the study (1996-1997), baseline erosions evaluated in 1979, Steinbrocker functional class in 1996-1997, polyarticular course of JCA, and history of systemic steroid treatment for more than 1 year were significantly associated with reduced BMD. In linear regression analysis including both the JCA and control groups, presence of JCA proved to be the factor most strongly associated with reduced BMD, explaining approximately 20% of its variation. CONCLUSION: Reduced BMD and evidence of increased bone turnover suggest that JCA patients may be at risk of developing premature osteoporosis and associated fractures later in life. The data are consistent with the concept that BMD in JCA is determined by many factors.  (+info)

Molecular fingerprinting reveals non-overlapping T cell oligoclonality between an inflamed site and peripheral blood. (4/962)

We have demonstrated a stable expansion of CD8+ T cells in the peripheral blood of a child with chronic arthritis. The expanded TCRBV family (TCRBV14) was enriched for CD57hiCD28- T cells. Sequencing of the TCRBV14 amplification products showed a TCR sequence which contributed 32% of the total TCR in the CD8+TCRBV14 population. Using the modified heteroduplex technique, the CD8+TCRBV14 cells showed a clonal pattern and these bands were restricted to the CD28- population. This method also detected multiple other clones within the CD8+ population but few in the CD4+ cells. The dominant TCRBV14+ clone was not detectable in synovial fluid T cells from two inflamed joints by CDR3 length analysis or heteroduplex probing, suggesting that this long-lived clone is excluded from inflammatory sites. Synovial fluid T cells showed an unexpected discordance of the CD28 and CD57 phenotype compared to peripheral blood mononuclear cells. T cells from both inflamed joints both showed marked oligoclonality in all TCR families and had almost identical heteroduplex patterns. Taken together these data suggest that some clones are actively excluded from inflamed sites in juvenile chronic arthritis, yet the pattern of restricted T cell expansion is shared between sites of inflammation.  (+info)

Absence of association between interleukin 1 alpha and oligoarticular juvenile chronic arthritis in UK patients. (5/962)

OBJECTIVE: To determine whether interleukin 1 alpha (IL-1alpha) polymorphisms are associated with UK oligoarticular juvenile chronic arthritis (JCA). PATIENTS AND CONTROLS: A well-characterized population of 164 UK Caucasian oligo-JCA patients and a control panel of 173 unrelated healthy UK Caucasian individuals. METHODS: The IL-1alpha promoter mutation at -889 was examined using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. The cases and controls were also genotyped for an IL-1alpha intronic microsatellite repeat. RESULTS: No association was observed between IL-1alpha polymorphisms and UK oligoarticular JCA patients. In particular, no association between IL-1alpha polymorphisms and chronic anterior uveitis was found. CONCLUSIONS: IL-1alpha is not associated with oligoarticular JCA in UK patients. This differs markedly to findings for IL-1alpha in Norwegian JCA patients.  (+info)

Responsiveness of outcome measures in juvenile chronic arthritis. Italian Pediatric Rheumatology Study Group. (6/962)

OBJECTIVE: To examine the responsiveness of the disease activity measures more commonly used in juvenile chronic arthritis (JCA) clinical trials. METHODS: Data were obtained from an open-label, non-controlled, multicentre trial designed to investigate the efficacy of methotrexate (MTX) in children with JCA. Outcome measures, including physician and parent global assessments, functional ability measures, articular variables, and laboratory indicators of systemic inflammation, were assessed at baseline and after 6 months of MTX treatment in 132 patients. Responsiveness of endpoint variables was evaluated by assessing the effect size (ES) and the standardized response median (SRM). RESULTS: Physician and parent global assessments were the more responsive instruments, showing ES and SRM above 1.0. Erythrocyte sedimentation rate, C-reactive protein, functional status measures and articular variables showed intermediate responsiveness. Morning stiffness, haemoglobin and platelet count were the least responsive instruments. CONCLUSION: The results of our analysis indicate that subjective estimations of the disease activity, either by the physician or parents, are the most responsive instruments in the assessment of the therapeutic response in children with JCA. The responsiveness of outcome measures in JCA should be further investigated in prospective controlled studies.  (+info)

Assessment of mutilans-like hand deformities in chronic inflammatory joint diseases. A radiographic study of 52 patients. (7/962)

OBJECTIVES: To evaluate patients with mutilans-like hand deformities in chronic inflammatory joint diseases and to determine radiographic scoring systems for arthritis mutilans (AM). METHODS: A total of 52 patients with severe hand deformities were collected during 1997. A Larsen hand score of 0-110 was formed to describe destruction of the hand joints. Secondly, each ray of the hand was assessed individually by summing the Larsen grade of the wrist and the grades of the MCP and PIP joints. When the sum of these grades was > or = 13, the finger was considered to be mutilated. A mutilans hand score of 0-10 was formed according to the number of mutilans fingers. Surgical treatment and spontaneous fusions were recorded. RESULTS: The study consisted of 22 patients with juvenile rheumatoid arthritis (JRA), nine with rheumatoid factor (RF) positive and 13 with RF negative arthritis, 27 patients with RF positive RA, and three adult patients with other diagnoses. The mean age of patients with adult rheumatic diseases was 27 years at the onset of arthritis. The mean disease duration in all patients was 30 years. The mean Larsen hand score was 93. Four patients had no mutilans fingers and in 15 patients all 10 fingers were mutilated. The Larsen hand score of 0-110 and the mutilans hand score of 0-10 correlated well (rs = 0.90). Fourteen patients showed spontaneous fusions in the peripheral joints. A total of 457 operations were performed on 48 patients. CONCLUSION: Both the Larsen hand score of 0-110 and the mutilans hand score of 0-10 improve accuracy in evaluating mutilans-like hand deformities, but in unevenly distributed hand deformities the mutilans hand score is better in describing deformation of individual fingers.  (+info)

Polymorphic haplotypes of the interleukin-10 5' flanking region determine variable interleukin-10 transcription and are associated with particular phenotypes of juvenile rheumatoid arthritis. (8/962)

OBJECTIVE: To determine the distribution of the interleukin-10 (IL-10) 5' flanking region haplotypes in children with arthritis and in controls, and to investigate the functional significance of each haplotype. METHODS: Sequence-specific oligonucleotide probing was used to determine haplotype frequency. Transient transfection studies were used to investigate the transcription of reporter genes driven by each haplotype. Whole blood cultures were performed to assess IL-10 production by each genotype. RESULTS: Patients with arthritis involving >4 joints were more likely to have a genotype with an ATA haplotype than those whose arthritis remained restricted to <4 joints. This ATA haplotype was associated with lower transcriptional activity than the GCC haplotype (P = 0.02), and the ATA/ATA genotype was associated with lower IL-10 production under lipopolysaccharide stimulation than other genotypes (P < 0.02). CONCLUSION: The results of this study demonstrate the functional significance of the ATA haplotype and reveal a significant association of genotypes containing this haplotype with extended oligoarthritis.  (+info)

There are several symptoms of RA, including:

1. Joint pain and stiffness, especially in the hands and feet
2. Swollen and warm joints
3. Redness and tenderness in the affected areas
4. Fatigue, fever, and loss of appetite
5. Loss of range of motion in the affected joints
6. Firm bumps of tissue under the skin (rheumatoid nodules)

RA can be diagnosed through a combination of physical examination, medical history, blood tests, and imaging studies such as X-rays or ultrasound. Treatment typically involves a combination of medications, including nonsteroidal anti-inflammatory drugs (NSAIDs), disease-modifying anti-rheumatic drugs (DMARDs), and biologic agents. Lifestyle modifications such as exercise and physical therapy can also be helpful in managing symptoms and improving quality of life.

There is no cure for RA, but early diagnosis and aggressive treatment can help to slow the progression of the disease and reduce symptoms. With proper management, many people with RA are able to lead active and fulfilling lives.

Osteoarthritis (OA) is a degenerative condition that occurs when the cartilage that cushions the joints breaks down over time, causing the bones to rub together. It is the most common form of arthritis and typically affects older adults.

Rheumatoid arthritis (RA) is an autoimmune condition that occurs when the body's immune system attacks the lining of the joints, leading to inflammation and pain. It can affect anyone, regardless of age, and is typically seen in women.

Other types of arthritis include psoriatic arthritis, gouty arthritis, and lupus-related arthritis. Treatment for arthritis depends on the type and severity of the condition, but can include medications such as pain relievers, anti-inflammatory drugs, and disease-modifying anti-rheumatic drugs (DMARDs). Physical therapy and lifestyle changes, such as exercise and weight loss, can also be helpful. In severe cases, surgery may be necessary to repair or replace damaged joints.

Arthritis is a leading cause of disability worldwide, affecting over 50 million adults in the United States alone. It can have a significant impact on a person's quality of life, making everyday activities such as walking, dressing, and grooming difficult and painful. Early diagnosis and treatment are important to help manage symptoms and slow the progression of the disease.

These animal models allow researchers to study the underlying causes of arthritis, test new treatments and therapies, and evaluate their effectiveness in a controlled environment before moving to human clinical trials. Experimental arthritis models are used to investigate various aspects of the disease, including its pathophysiology, immunogenicity, and potential therapeutic targets.

Some common experimental arthritis models include:

1. Collagen-induced arthritis (CIA): This model is induced in mice by immunizing them with type II collagen, which leads to an autoimmune response and inflammation in the joints.
2. Rheumatoid arthritis (RA) models: These models are developed by transferring cells from RA patients into immunodeficient mice, which then develop arthritis-like symptoms.
3. Osteoarthritis (OA) models: These models are induced in animals by subjecting them to joint injury or overuse, which leads to degenerative changes in the joints and bone.
4. Psoriatic arthritis (PsA) models: These models are developed by inducing psoriasis in mice, which then develop arthritis-like symptoms.

Experimental arthritis models have contributed significantly to our understanding of the disease and have helped to identify potential therapeutic targets for the treatment of arthritis. However, it is important to note that these models are not perfect representations of human arthritis and should be used as tools to complement, rather than replace, human clinical trials.

A type of arthritis that is caused by an infection in the joint, typically bacterial or viral. The most common form of infectious arthritis is Lyme disease, which is caused by the bacterium Borrelia burgdorferi and is transmitted through the bite of an infected blacklegged tick. Other types of infectious arthritis include septic arthritis (caused by bacterial infection) and reactive arthritis (caused by a bacterial or viral infection in another part of the body).

Symptoms: Pain, swelling, redness, warmth, and limited range of motion in the affected joint. Fever may also be present.

Diagnosis: A diagnosis is made based on symptoms, physical examination, blood tests (such as a complete blood count or a polymerase chain reaction test to detect the presence of bacteria or viruses), and imaging studies (such as X-rays or ultrasound).

Treatment: Treatment typically involves antibiotics to eradicate the infection, as well as medication to manage symptoms such as pain and inflammation. In severe cases, surgery may be necessary to repair damaged tissue or joints.

There are several types of JA, including:

1. Systemic juvenile idiopathic arthritis (SJIA): A severe form of JA that affects the entire body, causing fever, rash, and swollen lymph nodes in addition to joint inflammation.
2. Polyarticular juvenile idiopathic arthritis (PJIA): A common form of JA that affects multiple joints, especially in the hands and feet.
3. Oligoarticular juvenile idiopathic arthritis (OJIA): A mild form of JA that affects only a few joints.
4. Juvenile psoriatic arthritis (JPsA): A type of JA that is associated with psoriasis, a skin condition characterized by red, scaly patches.
5. Enthesitis-related juvenile idiopathic arthritis (ER-JIA): A rare form of JA that affects the areas where tendons and ligaments attach to bones.
6. Undifferentiated arthritis: A type of JA that does not fit into any of the other categories.

The symptoms of JA can vary depending on the specific type and severity of the condition, but may include:

* Joint pain and stiffness
* Swelling and redness in the affected joints
* Fatigue and fever
* Loss of mobility and range of motion
* Difficulty walking or standing

The exact cause of JA is not known, but it is believed to involve a combination of genetic and environmental factors. There is no cure for JA, but treatment options are available to help manage symptoms and prevent long-term joint damage. These may include medications such as nonsteroidal anti-inflammatory drugs (NSAIDs) and disease-modifying anti-rheumatic drugs (DMARDs), as well as physical therapy and lifestyle modifications.

There are five types of PsA:

1. Asymptomatic psoriatic arthritis - This type of psoriatic arthritis does not cause any symptoms and is typically diagnosed during routine blood tests or imaging studies.

2. Symptomatic psoriatic arthritis - This type of psoriatic arthritis causes painful joints, stiffness, and swelling in the hands and feet.

3. Distal interphalangeal predominant psoriatic arthritis - This type of psoriatic arthritis affects the joints at the tips of the fingers and toes.

4. Polyarticular psoriatic arthritis - This type of psoriatic arthritis causes inflammation in multiple joints throughout the body, including the hands, feet, knees, elbows, and spine.

5. Sulfur-shoulder psoriatic arthritis - This type of psoriatic arthritis primarily affects the shoulders and upper back.

Symptoms of PsA may include:

1. Joint pain and stiffness

2. Swollen and warm joints

3. Redness and warmth in the affected area

4. Fatigue

5. Low-grade fever

6. Loss of range of motion

7. Skin rashes or lesions

PsA is diagnosed based on a combination of physical examination, medical history, and laboratory tests such as blood tests to check for inflammatory markers (e.g., ESR and CRP) and X-rays or imaging studies to assess joint damage. There is no cure for PsA, but various treatments can help manage symptoms, slow the progression of the disease, and improve quality of life. These may include medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and disease-modifying anti-rheumatic drugs (DMARDs) or biologic agents that target specific proteins involved in inflammation. In severe cases, surgery may be necessary to repair damaged joints or correct deformities.

It's important for people with PsA to work closely with their healthcare provider to develop a personalized treatment plan that addresses their individual needs and monitors their disease activity over time. With appropriate treatment and self-care, many people with PsA are able to manage their symptoms, maintain joint function, and lead active and fulfilling lives.

In conclusion, psoriatic arthritis (PsA) is a chronic inflammatory disease that affects both the skin and joints, causing pain, stiffness, and swelling in various parts of the body. Early diagnosis and appropriate treatment can help manage symptoms, slow the progression of the disease, and improve quality of life.

Causes:

Reactive arthritis is caused by an immune system response to an infection or inflammation in another part of the body. Common causes include bacterial infections such as chlamydia, salmonella, and Campylobacter, as well as viral infections such as HIV and hepatitis B.

Symptoms:

Symptoms of reactive arthritis typically develop within 2-4 weeks after the initial infection or inflammation. They can include:

Pain and stiffness in the affected joints, particularly in the knees, ankles, and feet
Swelling, redness, and warmth in the affected joints
Loss of range of motion and flexibility in the affected joints
Fatigue and general feeling of illness

Diagnosis:

To diagnose reactive arthritis, a healthcare provider will typically begin with a physical examination and medical history. They may also order additional tests to rule out other conditions and confirm the presence of an underlying infection or inflammation. These tests can include:

Blood tests to check for the presence of antibodies or other signs of infection
Joint fluid tests to check for the presence of bacteria or other signs of inflammation
Imaging studies such as X-rays or magnetic resonance imaging (MRI) to rule out other conditions and assess joint damage

Treatment:

The goal of treatment for reactive arthritis is to reduce inflammation, relieve pain, and improve range of motion and flexibility in the affected joints. Treatment can include:

Antibiotics to treat any underlying bacterial infections
Nonsteroidal anti-inflammatory drugs (NSAIDs) to relieve pain and reduce inflammation
Corticosteroids to reduce inflammation and swelling in the affected joints
Physical therapy to improve range of motion and flexibility in the affected joints
Joint aspiration to drain fluid from the affected joint and relieve pressure
In severe cases, surgery may be necessary to repair or replace damaged joints.

Gouty arthritis can cause sudden and severe pain, swelling, redness, and warmth in the affected joint, which can last for several days before subsiding. Attacks can be triggered by factors such as alcohol consumption, certain foods (like meat or seafood), stress, and certain medications.

Gouty arthritis is caused by a combination of genetic and lifestyle factors, including a diet high in purine-rich foods, obesity, alcoholism, and certain medical conditions such as hypertension or kidney disease. It can be difficult to diagnose gouty arthritis because the symptoms are similar to other forms of arthritis, but blood tests can help confirm the presence of uric acid crystals in the joint fluid.

Treatment for gouty arthritis typically involves medications to reduce inflammation and relieve pain, as well as lifestyle changes such as limiting alcohol intake and following a low-purine diet. In some cases, corticosteroids or other medications may be prescribed to help reduce inflammation and prevent future attacks.

Previous Post Definition of 'Arthritis' in the medical field.

There are several possible causes of synovitis, including:

1. Infection: Bacterial, viral, or fungal infections can cause synovitis.
2. Autoimmune disorders: Conditions such as rheumatoid arthritis, psoriatic arthritis, and gout can cause chronic synovitis.
3. Overuse injuries: Repetitive strain injuries, such as those caused by repetitive jumping or throwing, can lead to synovitis in the affected joint.
4. Trauma: A sudden injury, such as a fall or a blow to the joint, can cause acute synovitis.

Symptoms of synovitis may include:

1. Pain: Pain is the most common symptom of synovitis, and it can range from mild to severe.
2. Swelling: The affected joint or limb may become swollen and warm to the touch.
3. Limited range of motion: Synovitis can cause stiffness and limited mobility in the affected joint.
4. Redness: The affected area may become red and inflamed.
5. Fever: In some cases, synovitis may be accompanied by a fever.

Treatment for synovitis depends on the underlying cause and the severity of the condition. Conservative treatments such as rest, physical therapy, and anti-inflammatory medications are often effective in managing mild to moderate cases of synovitis. In more severe cases, surgical intervention may be necessary.

In conclusion, synovitis is a common condition that can cause pain and limited mobility in the affected joint or limb. It is important to seek medical attention if symptoms persist or worsen over time, as early diagnosis and treatment can help to prevent long-term damage and improve outcomes.

The exact cause of osteoarthritis is not known, but it is thought to be due to a combination of factors such as genetics, wear and tear on joints over time, and injuries or trauma to the joint. Osteoarthritis can affect any joint in the body, but it most commonly affects the hands, knees, hips, and spine.

The symptoms of osteoarthritis can vary depending on the severity of the condition and which joint is affected. Common symptoms include:

* Pain or tenderness in the joint
* Stiffness, especially after periods of rest or inactivity
* Limited mobility or loss of flexibility
* Grating or crackling sensations when the joint is moved
* Swelling or redness in the affected joint
* Muscle weakness or wasting

There is no cure for osteoarthritis, but there are several treatment options available to manage the symptoms and slow the progression of the disease. These include:

* Pain relief medications such as acetaminophen or nonsteroidal anti-inflammatory drugs (NSAIDs)
* Physical therapy to improve mobility and strength
* Lifestyle modifications such as weight loss, regular exercise, and avoiding activities that exacerbate the condition
* Bracing or orthotics to support the affected joint
* Corticosteroid injections or hyaluronic acid injections to reduce inflammation and improve joint function
* Joint replacement surgery in severe cases where other treatments have failed.

Early diagnosis and treatment of osteoarthritis can help manage symptoms, slow the progression of the disease, and improve quality of life for individuals with this condition.

1. Rheumatoid arthritis (RA): An autoimmune disease that causes inflammation in the joints, leading to pain, stiffness, and swelling.
2. Osteoarthritis (OA): A degenerative condition that occurs when the cartilage in the joints wears down over time, causing pain and stiffness.
3. Psoriatic arthritis (PsA): An inflammatory disease that affects both the skin and joints, often occurring in people with psoriasis.
4. Ankylosing spondylitis (AS): A condition that causes inflammation in the spine and peripheral joints, leading to stiffness and pain.
5. Lupus: An autoimmune disease that can affect multiple systems in the body, including the joints, skin, and kidneys.
6. Juvenile idiopathic arthritis (JIA): A condition that affects children under the age of 16, causing inflammation in the joints and potentially leading to long-term complications.
7. Sjogren's syndrome: An autoimmune disorder that affects the glands that produce tears and saliva, causing dryness in the eyes and mouth.
8. Fibromyalgia: A condition characterized by widespread pain, fatigue, and sleep disturbances.
9. Gout: A type of inflammatory arthritis caused by excessive levels of uric acid in the blood, leading to sudden and severe attacks of joint pain.
10. Osteoporosis: A condition characterized by brittle bones and an increased risk of fractures, often occurring in older adults.

Rheumatic diseases can be challenging to diagnose and treat, as they often involve complex symptoms and a range of possible causes. However, with the help of rheumatology specialists and advanced diagnostic tools, it is possible to manage these conditions effectively and improve quality of life for patients.

Spondylitis, ankylosing can affect any part of the spine, but it most commonly affects the lower back (lumbar spine) and the neck (cervical spine). The condition can also affect other joints, such as the hips, shoulders, and feet.

The exact cause of spondylitis, ankylosing is not known, but it is believed to be an autoimmune disorder, meaning that the body's immune system mistakenly attacks healthy tissue in the joints. Genetics may also play a role in the development of the condition.

Symptoms of spondylitis, ankylosing can include:

* Back pain and stiffness
* Pain and swelling in the joints
* Limited mobility and flexibility
* Redness and warmth in the affected area
* Fatigue

If you suspect that you or someone you know may have spondylitis, ankylosing, it is important to seek medical attention for proper diagnosis and treatment. A healthcare professional can perform a physical examination and order imaging tests, such as X-rays or MRIs, to confirm the diagnosis and rule out other conditions.

Treatment for spondylitis, ankylosing typically involves a combination of medications and physical therapy. Medications may include nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and disease-modifying anti-rheumatic drugs (DMARDs). Physical therapy can help improve mobility and flexibility, as well as strengthen the muscles supporting the affected joints.

In severe cases of spondylitis, ankylosing, surgery may be necessary to repair or replace damaged joints. In some cases, the condition may progress to the point where the joints become fused and immobile, a condition known as ankylosis.

While there is no cure for spondylitis, ankylosing, early diagnosis and appropriate treatment can help manage symptoms and slow the progression of the disease. With proper care and support, individuals with spondylitis, ankylosing can lead active and fulfilling lives.

Examples of autoimmune diseases include:

1. Rheumatoid arthritis (RA): A condition where the immune system attacks the joints, leading to inflammation, pain, and joint damage.
2. Lupus: A condition where the immune system attacks various body parts, including the skin, joints, and organs.
3. Hashimoto's thyroiditis: A condition where the immune system attacks the thyroid gland, leading to hypothyroidism.
4. Multiple sclerosis (MS): A condition where the immune system attacks the protective covering of nerve fibers in the central nervous system, leading to communication problems between the brain and the rest of the body.
5. Type 1 diabetes: A condition where the immune system attacks the insulin-producing cells in the pancreas, leading to high blood sugar levels.
6. Guillain-Barré syndrome: A condition where the immune system attacks the nerves, leading to muscle weakness and paralysis.
7. Psoriasis: A condition where the immune system attacks the skin, leading to red, scaly patches.
8. Crohn's disease and ulcerative colitis: Conditions where the immune system attacks the digestive tract, leading to inflammation and damage to the gut.
9. Sjögren's syndrome: A condition where the immune system attacks the glands that produce tears and saliva, leading to dry eyes and mouth.
10. Vasculitis: A condition where the immune system attacks the blood vessels, leading to inflammation and damage to the blood vessels.

The symptoms of autoimmune diseases vary depending on the specific disease and the organs or tissues affected. Common symptoms include fatigue, fever, joint pain, skin rashes, and swollen lymph nodes. Treatment for autoimmune diseases typically involves medication to suppress the immune system and reduce inflammation, as well as lifestyle changes such as dietary changes and stress management techniques.

Rheumatoid nodules are caused by inflammation in the body, which can lead to the formation of abnormal tissue growths. They are more common in people with severe RA and can be a sign of active disease.

Rheumatoid nodules can be diagnosed through a physical examination and imaging tests such as ultrasound or MRI. Treatment options for rheumatoid nodules include medications to reduce inflammation, corticosteroids, and surgery to remove the nodule.

It is important to seek medical attention if you notice a new nodule or if an existing nodule changes in size, shape, or color, as this can be a sign of active disease.

1) They share similarities with humans: Many animal species share similar biological and physiological characteristics with humans, making them useful for studying human diseases. For example, mice and rats are often used to study diseases such as diabetes, heart disease, and cancer because they have similar metabolic and cardiovascular systems to humans.

2) They can be genetically manipulated: Animal disease models can be genetically engineered to develop specific diseases or to model human genetic disorders. This allows researchers to study the progression of the disease and test potential treatments in a controlled environment.

3) They can be used to test drugs and therapies: Before new drugs or therapies are tested in humans, they are often first tested in animal models of disease. This allows researchers to assess the safety and efficacy of the treatment before moving on to human clinical trials.

4) They can provide insights into disease mechanisms: Studying disease models in animals can provide valuable insights into the underlying mechanisms of a particular disease. This information can then be used to develop new treatments or improve existing ones.

5) Reduces the need for human testing: Using animal disease models reduces the need for human testing, which can be time-consuming, expensive, and ethically challenging. However, it is important to note that animal models are not perfect substitutes for human subjects, and results obtained from animal studies may not always translate to humans.

6) They can be used to study infectious diseases: Animal disease models can be used to study infectious diseases such as HIV, TB, and malaria. These models allow researchers to understand how the disease is transmitted, how it progresses, and how it responds to treatment.

7) They can be used to study complex diseases: Animal disease models can be used to study complex diseases such as cancer, diabetes, and heart disease. These models allow researchers to understand the underlying mechanisms of the disease and test potential treatments.

8) They are cost-effective: Animal disease models are often less expensive than human clinical trials, making them a cost-effective way to conduct research.

9) They can be used to study drug delivery: Animal disease models can be used to study drug delivery and pharmacokinetics, which is important for developing new drugs and drug delivery systems.

10) They can be used to study aging: Animal disease models can be used to study the aging process and age-related diseases such as Alzheimer's and Parkinson's. This allows researchers to understand how aging contributes to disease and develop potential treatments.

Lyme disease is typically diagnosed based on a combination of physical symptoms, medical history, and laboratory tests. Treatment typically involves antibiotics, which can help to clear the infection and alleviate symptoms.

Prevention of Lyme disease involves protecting against tick bites by using insect repellents, wearing protective clothing when outdoors, and conducting regular tick checks. Early detection and treatment of Lyme disease can help to prevent long-term complications, such as joint inflammation and neurological problems.

In this definition, we have used technical terms such as 'bacterial infection', 'blacklegged tick', 'Borrelia burgdorferi', and 'antibiotics' to provide a more detailed understanding of the medical concept.

1. Osteoarthritis: A degenerative condition that causes the breakdown of cartilage in the joints, leading to pain, stiffness, and loss of mobility.
2. Rheumatoid arthritis: An autoimmune disease that causes inflammation in the joints, leading to pain, swelling, and deformity.
3. Gout: A condition caused by the buildup of uric acid in the joints, leading to sudden and severe attacks of pain, inflammation, and swelling.
4. Bursitis: Inflammation of the bursae, small fluid-filled sacs that cushion the joints and reduce friction between tendons and bones.
5. Tendinitis: Inflammation of the tendons, which connect muscles to bones.
6. Synovitis: Inflammation of the synovial membrane, a thin lining that covers the joints and lubricates them with fluid.
7. Periarthritis: Inflammation of the tissues around the joints, such as the synovial membrane, tendons, and ligaments.
8. Spondyloarthritis: A group of conditions that affect the spine and sacroiliac joints, leading to inflammation and pain in these areas.
9. Juvenile idiopathic arthritis: A condition that affects children and causes inflammation and pain in the joints.
10. Systemic lupus erythematosus: An autoimmune disease that can affect many parts of the body, including the joints.

These are just a few examples of the many types of joint diseases that exist. Each type has its own unique symptoms and causes, and they can be caused by a variety of factors such as genetics, injury, infection, or age-related wear and tear. Treatment options for joint diseases can range from medication and physical therapy to surgery, depending on the severity of the condition and its underlying cause.

The exact cause of spondylarthropathies is not known, but they are believed to be an autoimmune response, where the body's immune system mistakenly attacks healthy tissues in the joints and spine. Genetics also play a role in the development of these conditions, as they tend to run in families.

There is no cure for spondylarthropathies, but various treatments can help manage symptoms and slow down the progression of the disease. These may include medications such as nonsteroidal anti-inflammatory drugs (NSAIDs) and disease-modifying anti-rheumatic drugs (DMARDs), physical therapy, and lifestyle modifications such as regular exercise and a healthy diet. In severe cases, surgery may be necessary to repair or replace damaged joints or spine.

Early diagnosis and treatment of spondylarthropathies are important to manage symptoms and prevent long-term complications such as permanent joint damage, loss of flexibility, and reduced lung function. If you experience persistent back pain or stiffness, it is essential to consult a healthcare professional for proper evaluation and diagnosis.

Psoriasis can affect any part of the body, including the scalp, elbows, knees, and lower back. The symptoms of psoriasis can vary in severity, and the condition can have a significant impact on quality of life. In addition to physical discomfort, psoriasis can also cause emotional distress and stigma.

There is no cure for psoriasis, but there are several treatment options available, including topical creams and ointments, light therapy, and systemic medications such as biologic drugs. With proper treatment, many people with psoriasis are able to manage their symptoms and improve their quality of life.

Psoriasis is relatively common, affecting approximately 2-3% of the global population, with a higher prevalence in Caucasians than in other races. It can occur at any age, but typically starts in the late teenage years or early adulthood. Psoriasis is often associated with other health conditions, such as diabetes, heart disease, and depression.

Overall, psoriasis is a complex and multifactorial condition that requires a comprehensive approach to management, including both physical and emotional support. With appropriate treatment and self-care, people with psoriasis can lead full and active lives.

There are several key features of inflammation:

1. Increased blood flow: Blood vessels in the affected area dilate, allowing more blood to flow into the tissue and bringing with it immune cells, nutrients, and other signaling molecules.
2. Leukocyte migration: White blood cells, such as neutrophils and monocytes, migrate towards the site of inflammation in response to chemical signals.
3. Release of mediators: Inflammatory mediators, such as cytokines and chemokines, are released by immune cells and other cells in the affected tissue. These molecules help to coordinate the immune response and attract more immune cells to the site of inflammation.
4. Activation of immune cells: Immune cells, such as macrophages and T cells, become activated and start to phagocytose (engulf) pathogens or damaged tissue.
5. Increased heat production: Inflammation can cause an increase in metabolic activity in the affected tissue, leading to increased heat production.
6. Redness and swelling: Increased blood flow and leakiness of blood vessels can cause redness and swelling in the affected area.
7. Pain: Inflammation can cause pain through the activation of nociceptors (pain-sensing neurons) and the release of pro-inflammatory mediators.

Inflammation can be acute or chronic. Acute inflammation is a short-term response to injury or infection, which helps to resolve the issue quickly. Chronic inflammation is a long-term response that can cause ongoing damage and diseases such as arthritis, asthma, and cancer.

There are several types of inflammation, including:

1. Acute inflammation: A short-term response to injury or infection.
2. Chronic inflammation: A long-term response that can cause ongoing damage and diseases.
3. Autoimmune inflammation: An inappropriate immune response against the body's own tissues.
4. Allergic inflammation: An immune response to a harmless substance, such as pollen or dust mites.
5. Parasitic inflammation: An immune response to parasites, such as worms or fungi.
6. Bacterial inflammation: An immune response to bacteria.
7. Viral inflammation: An immune response to viruses.
8. Fungal inflammation: An immune response to fungi.

There are several ways to reduce inflammation, including:

1. Medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and disease-modifying anti-rheumatic drugs (DMARDs).
2. Lifestyle changes, such as a healthy diet, regular exercise, stress management, and getting enough sleep.
3. Alternative therapies, such as acupuncture, herbal supplements, and mind-body practices.
4. Addressing underlying conditions, such as hormonal imbalances, gut health issues, and chronic infections.
5. Using anti-inflammatory compounds found in certain foods, such as omega-3 fatty acids, turmeric, and ginger.

It's important to note that chronic inflammation can lead to a range of health problems, including:

1. Arthritis
2. Diabetes
3. Heart disease
4. Cancer
5. Alzheimer's disease
6. Parkinson's disease
7. Autoimmune disorders, such as lupus and rheumatoid arthritis.

Therefore, it's important to manage inflammation effectively to prevent these complications and improve overall health and well-being.

There are several types of edema, including:

1. Pitting edema: This type of edema occurs when the fluid accumulates in the tissues and leaves a pit or depression when it is pressed. It is commonly seen in the skin of the lower legs and feet.
2. Non-pitting edema: This type of edema does not leave a pit or depression when pressed. It is often seen in the face, hands, and arms.
3. Cytedema: This type of edema is caused by an accumulation of fluid in the tissues of the limbs, particularly in the hands and feet.
4. Edema nervorum: This type of edema affects the nerves and can cause pain, numbness, and tingling in the affected area.
5. Lymphedema: This is a condition where the lymphatic system is unable to properly drain fluid from the body, leading to swelling in the arms or legs.

Edema can be diagnosed through physical examination, medical history, and diagnostic tests such as imaging studies and blood tests. Treatment options for edema depend on the underlying cause, but may include medications, lifestyle changes, and compression garments. In some cases, surgery or other interventions may be necessary to remove excess fluid or tissue.

The symptoms of tenosynovitis can vary depending on the location of the affected tendon, but common symptoms include:

* Pain and tenderness in the affected area
* Swelling and redness in the affected area
* Stiffness and limited range of motion in the affected joint
* Difficulty moving the affected limb or joint
* Clicking or snapping sensation in the affected joint

Tenosynovitis can be caused by a variety of factors, including:

* Overuse or repetitive strain on the tendon
* Injury or trauma to the affected area
* Age-related wear and tear on the tendons
* Certain medical conditions, such as gout or rheumatoid arthritis

Treatment for tenosynovitis usually involves rest, physical therapy, and anti-inflammatory medications. In severe cases, surgery may be necessary to repair the damaged tendon. It is important to seek medical attention if symptoms persist or worsen over time, as untreated tenosynovitis can lead to chronic pain and limited mobility.

There are several different types of pain, including:

1. Acute pain: This type of pain is sudden and severe, and it usually lasts for a short period of time. It can be caused by injuries, surgery, or other forms of tissue damage.
2. Chronic pain: This type of pain persists over a long period of time, often lasting more than 3 months. It can be caused by conditions such as arthritis, fibromyalgia, or nerve damage.
3. Neuropathic pain: This type of pain results from damage to the nervous system, and it can be characterized by burning, shooting, or stabbing sensations.
4. Visceral pain: This type of pain originates in the internal organs, and it can be difficult to localize.
5. Psychogenic pain: This type of pain is caused by psychological factors such as stress, anxiety, or depression.

The medical field uses a range of methods to assess and manage pain, including:

1. Pain rating scales: These are numerical scales that patients use to rate the intensity of their pain.
2. Pain diaries: These are records that patients keep to track their pain over time.
3. Clinical interviews: Healthcare providers use these to gather information about the patient's pain experience and other relevant symptoms.
4. Physical examination: This can help healthcare providers identify any underlying causes of pain, such as injuries or inflammation.
5. Imaging studies: These can be used to visualize the body and identify any structural abnormalities that may be contributing to the patient's pain.
6. Medications: There are a wide range of medications available to treat pain, including analgesics, nonsteroidal anti-inflammatory drugs (NSAIDs), and muscle relaxants.
7. Alternative therapies: These can include acupuncture, massage, and physical therapy.
8. Interventional procedures: These are minimally invasive procedures that can be used to treat pain, such as nerve blocks and spinal cord stimulation.

It is important for healthcare providers to approach pain management with a multi-modal approach, using a combination of these methods to address the physical, emotional, and social aspects of pain. By doing so, they can help improve the patient's quality of life and reduce their suffering.

The term "systemic" refers to the fact that the disease affects multiple organ systems, including the skin, joints, kidneys, lungs, and nervous system. LES is a complex condition, and its symptoms can vary widely depending on which organs are affected. Common symptoms include fatigue, fever, joint pain, rashes, and swelling in the extremities.

There are several subtypes of LES, including:

1. Systemic lupus erythematosus (SLE): This is the most common form of the disease, and it can affect anyone, regardless of age or gender.
2. Discoid lupus erythematosus (DLE): This subtype typically affects the skin, causing a red, scaly rash that does not go away.
3. Drug-induced lupus erythematosus: This form of the disease is caused by certain medications, and it usually resolves once the medication is stopped.
4. Neonatal lupus erythematosus: This rare condition affects newborn babies of mothers with SLE, and it can cause liver and heart problems.

There is no cure for LES, but treatment options are available to manage the symptoms and prevent flares. Treatment may include nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, immunosuppressive medications, and antimalarial drugs. In severe cases, hospitalization may be necessary to monitor and treat the disease.

It is important for people with LES to work closely with their healthcare providers to manage their condition and prevent complications. With proper treatment and self-care, many people with LES can lead active and fulfilling lives.

The burden of chronic diseases is significant, with over 70% of deaths worldwide attributed to them, according to the World Health Organization (WHO). In addition to the physical and emotional toll they take on individuals and their families, chronic diseases also pose a significant economic burden, accounting for a large proportion of healthcare expenditure.

In this article, we will explore the definition and impact of chronic diseases, as well as strategies for managing and living with them. We will also discuss the importance of early detection and prevention, as well as the role of healthcare providers in addressing the needs of individuals with chronic diseases.

What is a Chronic Disease?

A chronic disease is a condition that lasts for an extended period of time, often affecting daily life and activities. Unlike acute diseases, which have a specific beginning and end, chronic diseases are long-term and persistent. Examples of chronic diseases include:

1. Diabetes
2. Heart disease
3. Arthritis
4. Asthma
5. Cancer
6. Chronic obstructive pulmonary disease (COPD)
7. Chronic kidney disease (CKD)
8. Hypertension
9. Osteoporosis
10. Stroke

Impact of Chronic Diseases

The burden of chronic diseases is significant, with over 70% of deaths worldwide attributed to them, according to the WHO. In addition to the physical and emotional toll they take on individuals and their families, chronic diseases also pose a significant economic burden, accounting for a large proportion of healthcare expenditure.

Chronic diseases can also have a significant impact on an individual's quality of life, limiting their ability to participate in activities they enjoy and affecting their relationships with family and friends. Moreover, the financial burden of chronic diseases can lead to poverty and reduce economic productivity, thus having a broader societal impact.

Addressing Chronic Diseases

Given the significant burden of chronic diseases, it is essential that we address them effectively. This requires a multi-faceted approach that includes:

1. Lifestyle modifications: Encouraging healthy behaviors such as regular physical activity, a balanced diet, and smoking cessation can help prevent and manage chronic diseases.
2. Early detection and diagnosis: Identifying risk factors and detecting diseases early can help prevent or delay their progression.
3. Medication management: Effective medication management is crucial for controlling symptoms and slowing disease progression.
4. Multi-disciplinary care: Collaboration between healthcare providers, patients, and families is essential for managing chronic diseases.
5. Health promotion and disease prevention: Educating individuals about the risks of chronic diseases and promoting healthy behaviors can help prevent their onset.
6. Addressing social determinants of health: Social determinants such as poverty, education, and employment can have a significant impact on health outcomes. Addressing these factors is essential for reducing health disparities and improving overall health.
7. Investing in healthcare infrastructure: Investing in healthcare infrastructure, technology, and research is necessary to improve disease detection, diagnosis, and treatment.
8. Encouraging policy change: Policy changes can help create supportive environments for healthy behaviors and reduce the burden of chronic diseases.
9. Increasing public awareness: Raising public awareness about the risks and consequences of chronic diseases can help individuals make informed decisions about their health.
10. Providing support for caregivers: Chronic diseases can have a significant impact on family members and caregivers, so providing them with support is essential for improving overall health outcomes.

Conclusion

Chronic diseases are a major public health burden that affect millions of people worldwide. Addressing these diseases requires a multi-faceted approach that includes lifestyle changes, addressing social determinants of health, investing in healthcare infrastructure, encouraging policy change, increasing public awareness, and providing support for caregivers. By taking a comprehensive approach to chronic disease prevention and management, we can improve the health and well-being of individuals and communities worldwide.

Explanation: Genetic predisposition to disease is influenced by multiple factors, including the presence of inherited genetic mutations or variations, environmental factors, and lifestyle choices. The likelihood of developing a particular disease can be increased by inherited genetic mutations that affect the functioning of specific genes or biological pathways. For example, inherited mutations in the BRCA1 and BRCA2 genes increase the risk of developing breast and ovarian cancer.

The expression of genetic predisposition to disease can vary widely, and not all individuals with a genetic predisposition will develop the disease. Additionally, many factors can influence the likelihood of developing a particular disease, such as environmental exposures, lifestyle choices, and other health conditions.

Inheritance patterns: Genetic predisposition to disease can be inherited in an autosomal dominant, autosomal recessive, or multifactorial pattern, depending on the specific disease and the genetic mutations involved. Autosomal dominant inheritance means that a single copy of the mutated gene is enough to cause the disease, while autosomal recessive inheritance requires two copies of the mutated gene. Multifactorial inheritance involves multiple genes and environmental factors contributing to the development of the disease.

Examples of diseases with a known genetic predisposition:

1. Huntington's disease: An autosomal dominant disorder caused by an expansion of a CAG repeat in the Huntingtin gene, leading to progressive neurodegeneration and cognitive decline.
2. Cystic fibrosis: An autosomal recessive disorder caused by mutations in the CFTR gene, leading to respiratory and digestive problems.
3. BRCA1/2-related breast and ovarian cancer: An inherited increased risk of developing breast and ovarian cancer due to mutations in the BRCA1 or BRCA2 genes.
4. Sickle cell anemia: An autosomal recessive disorder caused by a point mutation in the HBB gene, leading to defective hemoglobin production and red blood cell sickling.
5. Type 1 diabetes: An autoimmune disease caused by a combination of genetic and environmental factors, including multiple genes in the HLA complex.

Understanding the genetic basis of disease can help with early detection, prevention, and treatment. For example, genetic testing can identify individuals who are at risk for certain diseases, allowing for earlier intervention and preventive measures. Additionally, understanding the genetic basis of a disease can inform the development of targeted therapies and personalized medicine."


Yersinia Infections are typically diagnosed through a combination of physical examination, laboratory tests such as blood cultures, and imaging studies such as X-rays or CT scans. Treatment usually involves antibiotics, which can help clear the infection and manage symptoms.

Prevention of Yersinia Infections is difficult, but good hygiene practices, proper food handling and storage, and avoiding contact with contaminated fecal matter can help reduce the risk of transmission. Vaccines are not available for Yersinia infections.

Some common symptoms of Yersiniosis include fever, abdominal pain, diarrhea, vomiting, and rash. In severe cases, Yersinia infections can cause inflammation of the joints, spleen, and liver, as well as bacteremia (the presence of bacteria in the bloodstream) and meningitis (inflammation of the lining around the brain and spinal cord).

Yersinia Infections can be transmitted through contaminated food or water, contact with infected animals or people, and from mother to child during pregnancy or childbirth. People at higher risk for Yersiniosis include young children, older adults, pregnant women, and those with weakened immune systems.

Complications of Yersinia Infections can include reactive arthritis (arthritis that develops as a result of an infection), chronic kidney disease, and osteomyelitis (inflammation of the bone). In rare cases, Yersinia infections can lead to life-threatening complications such as septicemia (blood poisoning) or meningitis.

The word "arthralgia" comes from the Greek words "arthron," meaning joint, and "algos," meaning pain. It is often used interchangeably with the term "joint pain," but arthralgia specifically refers to a type of pain that is not caused by inflammation or injury.

Arthralgia can manifest in different ways, including:

1. Aching or dull pain in one or more joints
2. Sharp or stabbing pain in one or more joints
3. Pain that worsens with movement or weight-bearing activity
4. Pain that improves with rest
5. Pain that is localized to one joint or multiple joints
6. Pain that is accompanied by stiffness or limited range of motion
7. Pain that is worse in the morning or after periods of rest
8. Pain that is triggered by certain activities or movements

The diagnosis of arthralgia typically involves a comprehensive medical history and physical examination, as well as diagnostic tests such as X-rays, blood tests, or imaging studies. Treatment for arthralgia depends on the underlying cause and may include medications, lifestyle modifications, or other interventions.

The symptoms of spondylarthritis can vary, but may include:

* Back pain that improves with exercise
* Stiffness in the neck or lower back
* Painful joints in the hips or shoulders
* Reduced range of motion in the affected joints
* Fatigue
* Loss of appetite
* Fever
* Swollen lymph nodes

The exact cause of spondylarthritis is unknown, but it is thought to be an autoimmune disorder. This means that the immune system mistakenly attacks healthy tissue in the body, leading to inflammation and joint damage.

There is no cure for spondylarthritis, but medications and lifestyle changes can help manage the symptoms. Treatment options may include:

* Nonsteroidal anti-inflammatory drugs (NSAIDs) to reduce pain and inflammation
* Corticosteroids to reduce inflammation
* Disease-modifying anti-rheumatic drugs (DMARDs) to slow the progression of the disease
* Biologic agents to target specific proteins involved in the immune response
* Physical therapy to improve range of motion and strength
* Rest and exercise to manage fatigue

Early diagnosis and treatment can help manage the symptoms of spondylarthritis and prevent long-term complications such as joint damage or spinal fusion.

Source: Medical Dictionary for the Health Professions and Nursing © Farlex 2012.

There are several factors that can contribute to bone resorption, including:

1. Hormonal changes: Hormones such as parathyroid hormone (PTH) and calcitonin can regulate bone resorption. Imbalances in these hormones can lead to excessive bone resorption.
2. Aging: As we age, our bones undergo remodeling more frequently, leading to increased bone resorption.
3. Nutrient deficiencies: Deficiencies in calcium, vitamin D, and other nutrients can impair bone health and lead to excessive bone resorption.
4. Inflammation: Chronic inflammation can increase bone resorption, leading to bone loss and weakening.
5. Genetics: Some genetic disorders can affect bone metabolism and lead to abnormal bone resorption.
6. Medications: Certain medications, such as glucocorticoids and anticonvulsants, can increase bone resorption.
7. Diseases: Conditions such as osteoporosis, Paget's disease of bone, and bone cancer can lead to abnormal bone resorption.

Bone resorption can be diagnosed through a range of tests, including:

1. Bone mineral density (BMD) testing: This test measures the density of bone in specific areas of the body. Low BMD can indicate bone loss and excessive bone resorption.
2. X-rays and imaging studies: These tests can help identify abnormal bone growth or other signs of bone resorption.
3. Blood tests: Blood tests can measure levels of certain hormones and nutrients that are involved in bone metabolism.
4. Bone biopsy: A bone biopsy can provide a direct view of the bone tissue and help diagnose conditions such as Paget's disease or bone cancer.

Treatment for bone resorption depends on the underlying cause and may include:

1. Medications: Bisphosphonates, hormone therapy, and other medications can help slow or stop bone resorption.
2. Diet and exercise: A healthy diet rich in calcium and vitamin D, along with regular exercise, can help maintain strong bones.
3. Physical therapy: In some cases, physical therapy may be recommended to improve bone strength and mobility.
4. Surgery: In severe cases of bone resorption, surgery may be necessary to repair or replace damaged bone tissue.

The symptoms of Felty syndrome can vary in severity and may include:

* Rheumatoid arthritis with joint deformity and loss of function
* Chronic lung disease, such as interstitial fibrosis or emphysema
* Enlarged lymph nodes, particularly in the neck and axillae
* Fever
* Night sweats
* Weight loss
* Fatigue

Felty syndrome is caused by an abnormal immune response that leads to inflammation in the joints, lungs, and lymph nodes. It can be associated with other autoimmune disorders, such as Sjögren's syndrome or systemic lupus erythematosus.

The diagnosis of Felty syndrome is based on a combination of clinical findings, laboratory tests, and imaging studies. Laboratory tests may include blood tests to assess for inflammatory markers, such as erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP), as well as tests to assess joint damage and lung function. Imaging studies, such as X-rays or computed tomography (CT) scans, may be used to evaluate joint damage and lung disease.

There is no cure for Felty syndrome, but treatment can help manage the symptoms and slow the progression of the disease. Treatment options may include:

* Medications to reduce inflammation, such as nonsteroidal anti-inflammatory drugs (NSAIDs) or disease-modifying anti-rheumatic drugs (DMARDs)
* Corticosteroids to reduce inflammation and suppress the immune system
* Immunosuppressive medications, such as methotrexate or azathioprine, to suppress the immune system and prevent joint damage
* Biologic agents, such as infliximab or etanercept, to target specific proteins involved in the immune response and reduce inflammation
* Physical therapy to maintain joint mobility and strength
* Surgery to repair or replace damaged joints, such as hip or knee replacement

It is important for individuals with Felty syndrome to work closely with their healthcare provider to develop a personalized treatment plan that addresses their specific needs and helps manage their symptoms. With appropriate treatment, many individuals with Felty syndrome are able to lead active and productive lives.

Sjögren's syndrome can affect people of all ages, but it most commonly occurs in women between the ages of 40 and 60. The exact cause of the disorder is not known, but it is believed to be an autoimmune response, meaning that the immune system mistakenly attacks the glands as if they were foreign substances.

Symptoms of Sjögren's syndrome can vary in severity and may include:

* Dry mouth (xerostomia)
* Dry eyes (dry eye syndrome)
* Fatigue
* Joint pain
* Swollen lymph nodes
* Rash
* Sores on the skin
* Numbness or tingling in the hands and feet
* Sexual dysfunction

There is no cure for Sjögren's syndrome, but various treatments can help manage the symptoms. These may include:

* Medications to stimulate saliva production
* Eye drops to moisturize the eyes
* Mouthwashes to stimulate saliva production
* Pain relief medication for joint pain
* Anti-inflammatory medication to reduce swelling
* Immunosuppressive medication to suppress the immune system
* Hormone replacement therapy (HRT) to treat hormonal imbalances.

Sjögren's syndrome can also increase the risk of developing other autoimmune disorders, such as rheumatoid arthritis or lupus. It is important for people with Sjögren's syndrome to work closely with their healthcare provider to manage their symptoms and monitor their condition over time.

Gout can be caused by several factors including genetics, diet, obesity, alcohol consumption, and certain medical conditions like high blood pressure and kidney disease. Symptoms of gout typically include sudden and severe pain, swelling, redness, and warmth in the affected joint, often accompanied by fever.

Gout is diagnosed based on physical examination, medical history, and laboratory tests such as blood tests to check uric acid levels. Treatment for gout usually involves medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and colchicine to reduce inflammation and pain. In severe cases, hospitalization may be necessary to manage the condition.

Lifestyle modifications such as maintaining a healthy diet, losing weight if overweight or obese, limiting alcohol consumption, and staying hydrated can also help manage gout. In some cases, medications to lower uric acid levels such as allopurinol may be prescribed to prevent future attacks of gout.

Gout is a chronic condition that requires ongoing management to prevent complications such as joint damage and kidney stones. With proper treatment and lifestyle modifications, most people with gout can lead active and productive lives.

There are several types of spondylitis, including:

1. Ankylosing spondylitis (AS): This is the most common form of spondylitis and primarily affects the lower back. It can cause stiffness, pain, and reduced mobility in the spine.
2. Psoriatic arthritis (PsA): This type of spondylitis affects both the joints and the spine, causing inflammation and pain. It often occurs in people with psoriasis, a skin condition that causes red, scaly patches.
3. Enteropathic spondylitis: This is a rare form of spondylitis that occurs in people with inflammatory bowel disease (IBD), such as Crohn's disease or ulcerative colitis.
4. Undifferentiated spondylitis: This type of spondylitis does not fit into any other category and may be caused by a variety of factors.

The symptoms of spondylitis can vary depending on the specific type and severity of the condition, but may include:

1. Back pain that is worse with activity and improves with rest
2. Stiffness in the back, particularly in the morning or after periods of inactivity
3. Redness and warmth in the affected area
4. Swelling in the affected joints
5. Limited range of motion in the spine
6. Fatigue
7. Loss of appetite
8. Low-grade fever

Spondylitis can be diagnosed through a combination of physical examination, medical history, and imaging tests such as X-rays or MRIs. Treatment typically involves a combination of medication and lifestyle modifications, such as exercise, physical therapy, and stress management techniques. In severe cases, surgery may be necessary to repair or replace damaged joints or tissue.

It's important to note that spondylitis is a chronic condition, meaning it cannot be cured but can be managed with ongoing treatment and lifestyle modifications. With proper management, many people with spondylitis are able to lead active and fulfilling lives.

There are different types of osteitis, including:

1. Osteitis fibrosa: A benign condition characterized by the formation of fibrous tissue in the bone, which can cause pain and stiffness.
2. Osteitis multiformis: A chronic condition that causes multiple areas of bone inflammation, often seen in patients with rheumatoid arthritis or ankylosing spondylitis.
3. Osteitis pseudogout: A condition characterized by the deposition of crystals in the bone, which can cause episodes of sudden and severe joint pain.
4. Osteitis suppurativa: A chronic condition characterized by recurring abscesses or pockets of pus in the bone, often seen in patients with a history of skin infections.

Symptoms of osteitis can include pain, swelling, redness and warmth over the affected area. Treatment options may vary depending on the underlying cause, but may include antibiotics for infection, anti-inflammatory medications, or surgical intervention to drain abscesses or remove infected tissue.

Some common types of bone diseases include:

1. Osteoporosis: A condition characterized by brittle, porous bones that are prone to fracture.
2. Osteoarthritis: A degenerative joint disease that causes pain and stiffness in the joints.
3. Rheumatoid arthritis: An autoimmune disorder that causes inflammation and pain in the joints.
4. Bone cancer: A malignant tumor that develops in the bones.
5. Paget's disease of bone: A condition characterized by abnormal bone growth and deformity.
6. Osteogenesis imperfecta: A genetic disorder that affects the formation of bone and can cause brittle bones and other skeletal deformities.
7. Fibrous dysplasia: A rare condition characterized by abnormal growth and development of bone tissue.
8. Multiple myeloma: A type of cancer that affects the plasma cells in the bone marrow.
9. Bone cysts: Fluid-filled cavities that can form in the bones and cause pain, weakness, and deformity.
10. Bone spurs: Abnormal growths of bone that can form along the edges of joints and cause pain and stiffness.

Bone diseases can be diagnosed through a variety of tests, including X-rays, CT scans, MRI scans, and bone biopsies. Treatment options vary depending on the specific disease and can include medication, surgery, or a combination of both.

There are several types of disease susceptibility, including:

1. Genetic predisposition: This refers to the inherent tendency of an individual to develop a particular disease due to their genetic makeup. For example, some families may have a higher risk of developing certain diseases such as cancer or heart disease due to inherited genetic mutations.
2. Environmental susceptibility: This refers to the increased risk of developing a disease due to exposure to environmental factors such as pollutants, toxins, or infectious agents. For example, someone who lives in an area with high levels of air pollution may be more susceptible to developing respiratory problems.
3. Lifestyle susceptibility: This refers to the increased risk of developing a disease due to unhealthy lifestyle choices such as smoking, lack of exercise, or poor diet. For example, someone who smokes and is overweight may be more susceptible to developing heart disease or lung cancer.
4. Immune system susceptibility: This refers to the increased risk of developing a disease due to an impaired immune system. For example, people with autoimmune disorders such as HIV/AIDS or rheumatoid arthritis may be more susceptible to opportunistic infections.

Understanding disease susceptibility can help healthcare providers identify individuals who are at risk of developing certain diseases and provide preventive measures or early intervention to reduce the risk of disease progression. Additionally, genetic testing can help identify individuals with a high risk of developing certain diseases, allowing for earlier diagnosis and treatment.

In summary, disease susceptibility refers to the predisposition of an individual to develop a particular disease or condition due to various factors such as genetics, environment, lifestyle choices, and immune system function. Understanding disease susceptibility can help healthcare providers identify individuals at risk and provide appropriate preventive measures or early intervention to reduce the risk of disease progression.

The risk of developing osteoarthritis of the knee increases with age, obesity, and previous knee injuries or surgery. Symptoms of knee OA can include:

* Pain and stiffness in the knee, especially after activity or extended periods of standing or sitting
* Swelling and redness in the knee
* Difficulty moving the knee through its full range of motion
* Crunching or grinding sensations when the knee is bent or straightened
* Instability or a feeling that the knee may give way

Treatment for knee OA typically includes a combination of medication, physical therapy, and lifestyle modifications. Medications such as pain relievers, anti-inflammatory drugs, and corticosteroids can help manage symptoms, while physical therapy can improve joint mobility and strength. Lifestyle modifications, such as weight loss, regular exercise, and avoiding activities that exacerbate the condition, can also help slow the progression of the disease. In severe cases, surgery may be necessary to repair or replace the damaged joint.

Osteoarticular tuberculosis is typically diagnosed through a combination of physical examination, imaging studies such as X-rays or CT scans, and laboratory tests to detect the presence of Mycobacterium tuberculosis infection. Treatment typically involves a course of antibiotics for a period of at least six months, and surgical intervention may be necessary in some cases.

Preventive measures for osteoarticular tuberculosis include vaccination against tuberculosis, screening for the disease in high-risk populations such as those with weakened immune systems, and avoiding close contact with individuals who have active tuberculosis infections.

Some of the key features of osteoarticular tuberculosis include:

* Pain and swelling in the affected joint
* Limited mobility in the joint
* Fever, fatigue, and weight loss
* Night sweats and loss of appetite
* Presence of Mycobacterium tuberculosis infection in the joint fluid or tissue.

Osteoarticular tuberculosis can be challenging to diagnose and treat, as it may mimic other conditions such as osteoarthritis or rheumatoid arthritis. However, early detection and appropriate treatment can help prevent long-term joint damage and improve outcomes for patients with this condition.

Overall, osteoarticular tuberculosis is a serious form of tuberculosis that affects the bones and joints, causing pain, swelling, and limited mobility. Prompt diagnosis and treatment are essential to prevent long-term damage and improve outcomes for patients with this condition.

Examples of acquired foot deformities include:

1. Arthritis-related deformities: Arthritis can cause degenerative changes in the joints of the foot, leading to deformity and pain.
2. Bunion deformities: Bunions are bony growths that form on the side of the big toe joint, causing pain and discomfort.
3. Hammertoe deformities: Hammertoes are abnormal curvatures of the toe joints, which can cause pain and stiffness.
4. Clubfoot: Clubfoot is a congenital deformity in which the foot is twisted inward and downward, causing difficulty walking or standing.
5. Charcot foot: Charcot foot is a degenerative condition that affects the bones of the foot and ankle, leading to deformity and pain.
6. Plantar fasciitis: Plantar fasciitis is inflammation of the plantar fascia, a band of tissue that runs along the bottom of the foot, causing heel pain and stiffness.
7. Achilles tendinitis: Achilles tendinitis is inflammation of the Achilles tendon, which connects the calf muscle to the heel bone, causing pain and stiffness in the ankle and foot.
8. Sesamoiditis: Sesamoiditis is inflammation of the sesamoid bones, small bones located under the first metatarsal bone, causing pain and swelling under the big toe.
9. Gout: Gout is a type of arthritis that causes sudden and severe pain in the foot, particularly in the big toe.
10. Pneumaticulitis: Pneumaticulitis is inflammation of the small air sacs (pneumatocysts) in the bones of the foot, causing pain and swelling.

These are just a few of the many conditions that can cause foot pain. If you are experiencing persistent or severe foot pain, it is important to see a doctor for an accurate diagnosis and appropriate treatment.

Chondrocalcinosis is a type of calcifying disorder, which is a group of conditions characterized by the deposition of minerals such as calcium and phosphate in soft tissues. This condition can affect various joints in the body, including the hips, knees, shoulders, and elbows.

In this article, we will explore the definition, causes, symptoms, diagnosis, treatment, and prognosis of chondrocalcinosis. We will also discuss the surgical procedures used to treat this condition and the potential complications that can arise.

Definition of Chondrocalcinosis:

Chondrocalcinosis is a medical term that refers to the deposition of calcium pyrophosphate crystals within cartilage. This condition is also known as chondromalacia or calcifying joint disease. It is a type of calcifying disorder, which affects the cartilage in various joints throughout the body.

Causes of Chondrocalcinosis:

The exact cause of chondrocalcinosis is not fully understood, but it is believed to be related to aging, genetics, and certain medical conditions. Some risk factors for developing chondrocalcinosis include:

Age: The risk of developing chondrocalcinosis increases with age, with most cases occurring in people over the age of 50.

Family history: People with a family history of chondrocalcinosis are more likely to develop the condition.

Rheumatoid arthritis or osteoarthritis: These conditions can increase the risk of developing chondrocalcinosis.

Other medical conditions: Certain medical conditions, such as hypothyroidism and hyperparathyroidism, can increase the risk of developing chondrocalcinosis.

Symptoms of Chondrocalcinosis:

The symptoms of chondrocalcinosis can vary depending on the severity of the condition and the joints affected. Common symptoms include:

Pain: Pain is one of the most common symptoms of chondrocalcinosis, particularly in the affected joint.

Stiffness: Joint stiffness and limited range of motion can also occur as a result of chondrocalcinosis.

Swelling: Swelling in the affected joint is another common symptom of chondrocalcinosis.

Redness: The affected joint may become red and warm to the touch due to inflammation.

Crepitus: Crepitus, or a grinding sensation, may be felt in the affected joint as a result of the calcium pyrophosphate crystals rubbing against each other.

Treatment of Chondrocalcinosis:

There is no cure for chondrocalcinosis, but there are several treatment options available to manage the symptoms and slow down the progression of the condition. These may include:

Pain relief medication: Over-the-counter pain relievers such as acetaminophen or nonsteroidal anti-inflammatory drugs (NSAIDs) can help alleviate pain and reduce inflammation.

Physical therapy: Gentle exercises and stretches can help maintain joint mobility and strength.

Joint injections: Injecting corticosteroids or hyaluronic acid into the affected joint can help reduce inflammation and relieve pain.

Surgery: In severe cases of chondrocalcinosis, surgery may be necessary to remove the calcium pyrophosphate crystals or repair damaged tissue.

Prevention of Chondrocalcinosis:

There is no guaranteed way to prevent chondrocalcinosis, but there are several measures that can help reduce the risk of developing the condition. These may include:

Maintaining a healthy weight: Excessive weight can put additional strain on the joints and increase the risk of developing chondrocalcinosis.

Staying active: Regular exercise can help maintain joint mobility and strength, reducing the risk of developing chondrocalcinosis.

Wearing protective gear: Wearing protective gear such as knee pads or elbow pads when engaging in activities that involve repetitive stress on the joints can help reduce the risk of developing chondrocalcinosis.

Avoiding excessive stress on the joints: Avoiding activities that involve repetitive stress on the joints, such as heavy lifting or bending, can help reduce the risk of developing chondrocalcinosis.

Early diagnosis and treatment of chondrocalcinosis can help manage symptoms and slow down the progression of the condition. If you suspect you may have chondrocalcinosis, it is important to consult with a healthcare professional for proper evaluation and treatment.

Some common types of connective tissue diseases include:

1. Rheumatoid arthritis (RA): A chronic autoimmune disorder that causes inflammation and joint damage.
2. Systemic lupus erythematosus (SLE): An autoimmune disorder that can affect multiple systems in the body, including the skin, joints, and kidneys.
3. Sjogren's syndrome: An autoimmune disorder that causes dry eyes and mouth, as well as joint pain and swelling.
4. Fibromyalgia: A chronic condition characterized by widespread muscle pain and fatigue.
5. Myositis: Inflammatory diseases that affect the muscles, such as dermatomyositis and polymyositis.
6. Giant cell arteritis: A condition that causes inflammation of the blood vessels, particularly in the head and neck.
7. Takayasu arteritis: A condition that causes inflammation of the blood vessels in the aorta and its branches.
8. Polyarteritis nodosa: A condition that causes inflammation of the blood vessels, particularly in the hands and feet.
9. IgG4-related disease: A condition characterized by inflammation and damage to various organs, including the pancreas, salivary glands, and liver.

Connective tissue diseases can cause a wide range of symptoms, including joint pain and stiffness, fatigue, skin rashes, fever, and weight loss. Treatment options vary depending on the specific disease and its severity, but may include medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and disease-modifying anti-rheumatic drugs (DMARDs). In some cases, surgery or physical therapy may also be necessary.

Examples of acute diseases include:

1. Common cold and flu
2. Pneumonia and bronchitis
3. Appendicitis and other abdominal emergencies
4. Heart attacks and strokes
5. Asthma attacks and allergic reactions
6. Skin infections and cellulitis
7. Urinary tract infections
8. Sinusitis and meningitis
9. Gastroenteritis and food poisoning
10. Sprains, strains, and fractures.

Acute diseases can be treated effectively with antibiotics, medications, or other therapies. However, if left untreated, they can lead to chronic conditions or complications that may require long-term care. Therefore, it is important to seek medical attention promptly if symptoms persist or worsen over time.

There are several types of vasculitis, each with its own set of symptoms and characteristics. Some common forms of vasculitis include:

1. Giant cell arteritis: This is the most common form of vasculitis, and it affects the large arteries in the head, neck, and arms. Symptoms include fever, fatigue, muscle aches, and loss of appetite.
2. Takayasu arteritis: This type of vasculitis affects the aorta and its major branches, leading to inflammation in the blood vessels that supply the heart, brain, and other vital organs. Symptoms include fever, fatigue, chest pain, and shortness of breath.
3. Polymyalgia rheumatica: This is an inflammatory condition that affects the muscles and joints, as well as the blood vessels. It often occurs in people over the age of 50 and is frequently associated with giant cell arteritis. Symptoms include pain and stiffness in the shoulders, hips, and other joints, as well as fatigue and fever.
4. Kawasaki disease: This is a rare condition that affects children under the age of 5, causing inflammation in the blood vessels that supply the heart and other organs. Symptoms include high fever, rash, swollen lymph nodes, and irritability.

The exact cause of vasculitis is not fully understood, but it is thought to be an autoimmune disorder, meaning that the body's immune system mistakenly attacks its own blood vessels. Genetic factors may also play a role in some cases.

Diagnosis of vasculitis typically involves a combination of physical examination, medical history, and diagnostic tests such as blood tests, imaging studies (e.g., MRI or CT scans), and biopsies. Treatment options vary depending on the specific type of vasculitis and its severity, but may include medications to reduce inflammation and suppress the immune system, as well as lifestyle modifications such as exercise and stress management techniques. In severe cases, surgery or organ transplantation may be necessary.

In addition to these specific types of vasculitis, there are other conditions that can cause similar symptoms and may be included in the differential diagnosis, such as:

1. Rheumatoid arthritis (RA): This is a chronic autoimmune disorder that affects the joints and can cause inflammation in blood vessels.
2. Systemic lupus erythematosus (SLE): This is another autoimmune disorder that can affect multiple systems, including the skin, joints, and blood vessels.
3. Polyarteritis nodosa: This is a condition that causes inflammation of the blood vessels, often in association with hepatitis B or C infection.
4. Takayasu arteritis: This is a rare condition that affects the aorta and its branches, causing inflammation and narrowing of the blood vessels.
5. Giant cell arteritis: This is a condition that causes inflammation of the large and medium-sized blood vessels, often in association with polymyalgia rheumatica (PMR).
6. Kawasaki disease: This is a rare condition that affects children, causing inflammation of the blood vessels and potential heart complications.
7. Henoch-Schönlein purpura: This is a rare condition that causes inflammation of the blood vessels in the skin, joints, and gastrointestinal tract.
8. IgG4-related disease: This is a condition that can affect various organs, including the pancreas, bile ducts, and blood vessels, causing inflammation and potentially leading to fibrosis or tumor formation.

It is important to note that these conditions may have similar symptoms and signs as vasculitis, but they are distinct entities with different causes and treatment approaches. A thorough diagnostic evaluation, including laboratory tests and imaging studies, is essential to determine the specific diagnosis and develop an appropriate treatment plan.

Iritis, also known as anterior uveitis, is a type of inflammatory eye disease that affects the iris, which is the coloured part of the eye. It is a condition where the iris becomes inflamed, leading to pain, redness, and blurred vision.

Causes:

The exact cause of iritis is not known, but it is believed to be an autoimmune response, where the body's immune system mistakenly attacks healthy tissue in the eye. It can also be triggered by an infection or injury.

Symptoms:

The symptoms of iritis can vary depending on the severity of the condition, but common signs include:

* Eye pain, which can be severe
* Redness and inflammation of the eye
* Blurred vision or sensitivity to light
* Seeing floaters or flashes of light
* Sensitivity to touch or pressure on the eye

Diagnosis:

Iritis is diagnosed based on a comprehensive eye exam, which includes a visual acuity test, dilated eye exam, and tonometry. The doctor may also perform additional tests such as a fluorescein dye test or imaging studies to rule out other conditions.

Treatment:

The treatment of iritis typically involves a combination of medications and therapies, including:

* Corticosteroids to reduce inflammation
* Anti-inflammatory eye drops or ointments
* Pain relief medication
* Warm compresses to the affected eye
* Eye exercises to improve vision
* In severe cases, surgery may be necessary to remove the inflamed tissue

Prognosis:

The prognosis for iritis is generally good if treated promptly and effectively. However, if left untreated, it can lead to complications such as cataracts, glaucoma, or permanent vision loss. It is important to seek medical attention immediately if symptoms persist or worsen over time.

Prevention:

There is no known prevention for iritis, but early detection and treatment can help reduce the risk of complications. Regular eye exams and awareness of the signs and symptoms can help identify the condition in its early stages.

Complications:

Iritis can lead to several complications if left untreated or if the inflammation is not properly managed. These may include:

* Cataracts: The inflammation can cause clouding of the lens, leading to vision loss.
* Glaucoma: The increased pressure in the eye can lead to damage to the optic nerve and vision loss.
* Permanent vision loss: If the inflammation is not properly managed, it can lead to permanent vision loss.
* Increased risk of infection: Iritis can increase the risk of infection, particularly if the eye is not properly cleaned and cared for.

Conclusion:

Iritis is a painful and potentially sight-threatening condition that can cause inflammation in the iris of the eye. Early detection and prompt treatment are crucial to prevent complications and preserve vision. A comprehensive understanding of the signs, symptoms, diagnosis, treatment, prognosis, prevention, and complications of iritis is essential for effective management of this condition. If you suspect you or someone you know may have iritis, it is important to seek medical attention promptly to ensure proper diagnosis and treatment.

Anterior uveitis can be caused by a variety of factors, including infection, autoimmune disorders, and trauma. It is often diagnosed through a combination of physical examination, imaging tests such as ultrasound or MRI, and laboratory tests to rule out other conditions. Treatment options for anterior uveitis depend on the underlying cause and may include antibiotics, anti-inflammatory medications, and surgery to remove any affected tissue.

In summary, anterior uveitis is a type of inflammation that occurs in the front part of the eye, which can cause symptoms such as redness, pain, blurred vision, and sensitivity to light. It can be caused by a variety of factors and diagnosed through a combination of physical examination, imaging tests, and laboratory tests. Treatment options depend on the underlying cause and may include antibiotics, anti-inflammatory medications, and surgery.

1. Athlete's Foot (Tinea Pedis): A fungal infection that causes itching, burning, and cracking on the soles of the feet and between the toes.
2. Bunions: Bony growths on the side or base of the big toe, causing pain, redness, and swelling.
3. Corns and Calluses: Thickened areas of skin on the feet, often caused by poorly fitting shoes or repeated friction.
4. Plantar Fasciitis: Inflammation of the plantar fascia, a band of tissue that runs along the bottom of the foot, causing heel pain and stiffness.
5. Gout: A type of arthritis that causes sudden, severe pain in the feet and ankles, often accompanied by swelling and redness.
6. Hammertoes: Deformed toe joints, caused by poorly fitting shoes or muscle imbalance, leading to pain, corns, and calluses.
7. Ingrown toenails: Nails that grow into the skin, causing pain, redness, and swelling.
8. Osteoarthritis: Wear and tear on the joints of the feet, leading to pain, stiffness, and limited mobility.
9. Peripheral Neuropathy: Damage to the nerves in the feet, causing numbness, tingling, and pain.
10. Ulcers: Open sores on the skin of the feet, often caused by diabetes, poor circulation, or injury.

Foot diseases can be diagnosed through physical examination, imaging tests such as X-rays or CT scans, and laboratory tests to determine the cause of the condition. Treatment options vary depending on the specific disease, but may include medications, footwear modifications, orthotics, physical therapy, and in some cases, surgery.

There are several different types of uveitis, including:

1. Anterior uveitis: This type affects the front part of the eye and is the most common form of uveitis. It is often caused by an infection or injury.
2. Posterior uveitis: This type affects the back part of the eye and can be caused by a systemic disease such as sarcoidosis or juvenile idiopathic arthritis.
3. Intermediate uveitis: This type affects the middle layer of the eye and is often caused by an autoimmune disorder.
4. Panuveitis: This type affects the entire uvea and can be caused by a systemic disease such as vasculitis or Behçet's disease.

Symptoms of uveitis may include:

* Eye pain
* Redness and swelling in the eye
* Blurred vision
* Sensitivity to light
* Floaters (specks or cobwebs in your vision)
* Flashes of light

If you experience any of these symptoms, it is important to see an eye doctor as soon as possible. Uveitis can be diagnosed with a comprehensive eye exam, which may include imaging tests such as ultrasound or MRI. Treatment for uveitis depends on the cause and severity of the condition, but may include medication to reduce inflammation, antibiotics for infections, or surgery to remove any diseased tissue.

Early diagnosis and treatment are important to prevent complications such as cataracts, glaucoma, and blindness. If you have uveitis, it is important to follow your doctor's recommendations for treatment and monitoring to protect your vision.

There are several types of Mycoplasma bacteria that can cause infection in humans, including:

1. Mycoplasma pneumoniae, which is the most common cause of atypical pneumonia and can also cause sinus infections, bronchitis, and other respiratory infections.
2. Mycoplasma genitalium, which can cause pelvic inflammatory disease, epididymitis, and urethritis.
3. Mycoplasma hominis, which is a common inhabitant of the human respiratory tract and can cause infections such as pneumonia and bronchitis.
4. Mycoplasma fermentans, which is associated with respiratory infections and has been linked to conditions such as asthma and chronic obstructive pulmonary disease (COPD).

Mycoplasma infections are typically diagnosed through a combination of physical examination, medical history, and laboratory tests such as blood cultures and PCR (polymerase chain reaction) tests. Treatment for Mycoplasma infections usually involves antibiotics, but the type and duration of treatment may vary depending on the severity and location of the infection.

Prevention measures for Mycoplasma infections include good hygiene practices such as frequent handwashing, avoiding close contact with people who are sick, and covering the mouth and nose when coughing or sneezing. Vaccines are also available for some types of Mycoplasma bacteria, such as the M. pneumoniae vaccine, which is recommended for certain high-risk groups.

Overall, Mycoplasma infections can be serious and potentially life-threatening, especially in certain populations such as young children, older adults, and people with weakened immune systems. If you suspect that you or someone you know may have a Mycoplasma infection, it is important to seek medical attention right away.

The exact cause of PMR is not known, but it is believed to be related to an abnormal immune response. The condition often occurs in conjunction with another inflammatory disorder called giant cell arteritis (GCA), which affects the blood vessels.

Symptoms of PMR include:

* Pain and stiffness in the shoulders, hips, and other joints
* Fatigue
* Fever
* Loss of appetite
* Sleep disturbances
* Weight loss

The diagnosis of PMR is based on a combination of symptoms, physical examination findings, and laboratory test results. Laboratory tests may include blood tests to check for inflammatory markers, such as erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP).

Treatment for PMR typically involves a combination of medications, including:

* Corticosteroids to reduce inflammation
* Pain relievers, such as nonsteroidal anti-inflammatory drugs (NSAIDs) or narcotics
* Anti-inflammatory medications, such as disease-modifying anti-rheumatic drugs (DMARDs) or biologic response modifiers

In addition to medication, physical therapy and exercise may be helpful in managing the symptoms of PMR. In some cases, surgery may be necessary to repair joint damage.

The prognosis for PMR is generally good, with most people experiencing significant improvement within a few months of starting treatment. However, the condition can be challenging to diagnose and treat, and it is important to work closely with a healthcare provider to find the most effective treatment plan.

The term "osteomyelitis" comes from the Greek words "osteon," meaning bone, and "myelitis," meaning inflammation of the spinal cord. The condition is caused by an infection that spreads to the bone from another part of the body, such as a skin wound or a urinary tract infection.

There are several different types of osteomyelitis, including:

1. Acute osteomyelitis: This type of infection occurs suddenly and can be caused by bacteria such as Staphylococcus aureus or Streptococcus pneumoniae.
2. Chronic osteomyelitis: This type of infection develops slowly over time and is often caused by bacteria such as Mycobacterium tuberculosis.
3. Pyogenic osteomyelitis: This type of infection is caused by bacteria that enter the body through a skin wound or other opening.
4. Tubercular osteomyelitis: This type of infection is caused by the bacteria Mycobacterium tuberculosis and is often associated with tuberculosis.

Symptoms of osteomyelitis can include fever, chills, fatigue, swelling, redness, and pain in the affected area. Treatment typically involves antibiotics to fight the infection, as well as supportive care to manage symptoms and prevent complications. In severe cases, surgery may be necessary to remove infected tissue or repair damaged bone.

Preventing osteomyelitis involves taking steps to avoid infections altogether, such as practicing good hygiene, getting vaccinated against certain diseases, and seeking medical attention promptly if an infection is suspected.

Examples of delayed hypersensitivity reactions include contact dermatitis (a skin reaction to an allergic substance), tuberculin reactivity (a reaction to the bacteria that cause tuberculosis), and sarcoidosis (a condition characterized by inflammation in various organs, including the lungs and lymph nodes).

Delayed hypersensitivity reactions are important in the diagnosis and management of allergic disorders and other immune-related conditions. They can be detected through a variety of tests, including skin prick testing, patch testing, and blood tests. Treatment for delayed hypersensitivity reactions depends on the underlying cause and may involve medications such as antihistamines, corticosteroids, or immunosuppressants.

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A common lasting effect of JDM is childhood arthritis.[citation needed] [1] Archived July 5, 2008, at the Wayback Machine " ... Juvenile dermatomyositis (JDM) is an idiopathic inflammatory myopathy (IMM) of presumed autoimmune dysfunction resulting in ... "Juvenile Dermatomyositis (JDM)". Cincinnatichildrens.org. Retrieved 2015-09-27. (Webarchive template wayback links, Articles ... Feldman BM, Rider LG, Reed AM, Pachman LM (June 2008). "Juvenile dermatomyositis and other idiopathic inflammatory myopathies ...
ERAP1 with the enthesitis related arthritis subtype and IL23R with juvenile psoriatic arthritis". Arthritis Research & Therapy ... 173 polymorphism of the macrophage migration inhibitory factor gene in systemic-onset juvenile idiopathic arthritis". Arthritis ... Colbert RA (2010). "Classification of juvenile spondyloarthritis: Enthesitis-related arthritis and beyond". Nature Reviews ... Correlate with Disease Activity in the Enthesitis-related Arthritis Category of Juvenile Idiopathic Arthritis". The Journal of ...
He and colleagues first described the association of HLA-A2 with juvenile idiopathic arthritis. Along with Alan Rosenberg, he ... Roberton, D. M.; Cabral, D. A.; Malleson, P. N.; Petty, R. E. (1996). "Juvenile psoriatic arthritis: followup and evaluation of ... An association between HLA-A2 and juvenile rheumatoid arthritis in girls. J Rheumatol. 1982;9(6):916-920. Rosenberg AM, Petty ... These findings are now included in the juvenile idiopathic arthritis classification, proposed by the International League of ...
In 2008, her son was diagnosed with juvenile arthritis. She now raises funds for research. In The Sunday Times on 15 October ...
The field of juvenile idiopathic arthritis was her speciality. In the 1930s, Aitken was vice-dean of the Royal Free Hospital ... Janet Kerr Aitken CBE MD FRCP (1886 - 11 April 1982) was a specialist in juvenile rheumatism and President of the Medical ...
She has juvenile chronic arthritis and uses a wheelchair. She portrayed Alice in Richard Cameron's play Flower Girls, a play ...
As a child, Horiba suffered from juvenile rheumatoid arthritis. He attended Kyoto Teachers' School's Elementary School and ...
Cerna M, Vavrincova P, Havelka S, Ivaskova E, Stastny P (1994). "Class II alleles in juvenile arthritis in Czech children". J ... DRB1*1201 is associated with iritis in juvenile arthritis, primary antiphospholipid syndrome, tiopronin intolerance in ... 1994). "A possible linkage of HLA-DRB haplotypes with Tiopronin intolerance in rheumatoid arthritis". Clin. Exp. Rheumatol. 12 ... 2007). "Human Leukocyte Antigens in Undifferentiated Spondyloarthritis". Seminars in Arthritis and Rheumatism. 37 (3): 198-201 ...
Malleson, P; Schaller, JG; Dega, F; Cassidy, SB; Pagon, RA (September 1981). "Familial arthritis and camptodactyly". Arthritis ... Rotenstein D, Gibbas DL, Majmudar B, and Chastain EA: Familial Granulomatous Arteritis with Polyarthritis of Juvenile Onset. ... Arthritis and Rheumatism 2002; 46: 3041-3045. PMID 12428248. doi:10.1002/art.10618. Caso F, Galozzi P, Costa L, Sfriso P, ... doi:10.1016/0002-9343(85)90286-4. Malleson P, Schaller JG, Dega F, Cassidy SB, and Pagon RA : Familial Arthritis and ...
Less common symptoms include pyrexia, anorexia, and joint pain caused by sterile suppurative arthritis. The cause of juvenile ... Juvenile cellulitis, also known as puppy strangles or juvenile pyoderma, is an uncommon disease of dogs. Symptoms include ... Juvenile cellulitis". Muller & Kirk's small animal dermatology (7th ed.). St. Louis, Mo.: Elsevier. pp. 708-709. ISBN ... Park, C; Yoo, JH; Kim, HJ; Kang, BT; Park, HM (November 2010). "Combination of cyclosporin A and prednisolone for juvenile ...
Zeggini, E. (2002). "Tumour necrosis factor receptor II polymorphism and juvenile idiopathic arthritis". Rheumatology. 41 (4): ... She continued her studies on the immunogenetics of the major histocompatibility complex in childhood arthritis at the Arthritis ... Zeggini, Eleftheria (2002). Genetic dissection of the major histocompatibility complex in juvenile oligoarthritis. manchester. ...
Forero L, Zwirner NW, Fink CW, Fernández-Viña MA, Stastny P (1998). "Juvenile arthritis, HLA-A2 and binding of DEK oncogene- ... "Antibodies to the 45 kDa DEK nuclear antigen in pauciarticular onset juvenile rheumatoid arthritis and iridocyclitis: selective ... Arthritis Rheum. 41 (8): 1505-10. doi:10.1002/1529-0131(199808)41:8. 3.0.CO;2-N. PMID 9704652. Wichmann I, Garcia-Lozano JR, ...
All was well until her son Daniel developed juvenile arthritis. Being supported by Dr Richard Locke, Shula started an affair ...
At age of 10 he was diagnosed with juvenile arthritis. In 2016, Downey explains "I was a young boy with an old man's body. ...
skeletal: arthritis, from calcium pyrophosphate deposition in joints leading to joint pains. The most commonly affected joints ... GeneReview/NCBI/NIH/UW entry on TFR2-Related Hereditary Hemochromatosis GeneReview/NCBI/NIH/UW entry on Juvenile Hereditary ... The most common presentation is hepatic cirrhosis in combination with hypopituitarism, cardiomyopathy, diabetes, arthritis, or ...
Goldberg MA, Arnett FC, Bias WB, Shulman LE (1976). "Histocompatibility antigens in systemic lupus erythematosus". Arthritis ... or juvenile-onset myositis, with 4,724 control subjects. They found that multiple genes that make up AH8.1 define the genetic ...
... and juvenile rheumatoid arthritis with contractures. This means they have severe issues with all four limbs. In terms of ... juvenile rheumatoid arthritis (JRA) with contractures" As a functional class, ACSM's Primary Care Sports Medicine defines LAF1 ...
"Juvenile idiopathic arthritis classified by the ILAR criteria: HLA associations in UK patients". Rheumatology. Oct 2002. ... in the development of global consensus on the diagnosis of rheumatological diseases especially juvenile idiopathic arthritis It ... League of Associations for Rheumatology core endpoints for symptom modifying antirheumatic drugs in rheumatoid arthritis ...
The victim was believed between 30 and 60 years old at the time of her death and her body bore signs of arthritis in her back. ... On December 23, 2004, juveniles found a decomposed human skeleton in a barn in a wooded area near the intersection of US 69 and ... Other findings were a "prominent sternal fissure, healed nasal fracture, lumbar scoliosis, and arthritis". No cause of death ...
ISBN 978-1-4160-2999-1. Medical Glossary of the Spondylitis Association of America Pauciarticular juvenile rheumatoid arthritis ... February 2004). "International League of Associations for Rheumatology classification of juvenile idiopathic arthritis: second ... Oligoarthritis (from Greek oligos - 'few') is defined as arthritis affecting two to four joints during the first six months of ...
Then more than sixty years old, he was increasingly infirm with arthritis and failing eyesight. Girty returned to his farm in ... Joseph Altsheler features Simon Girty as a turncoat and villain in several of his "Young Trailer Series" of eight juvenile ...
... juvenile) 2, parkin (6q26) PCMT1: protein-L-isoaspartate (D-aspartate) O-methyltransferase (6q25.1) PERP: p53 apoptosis ... dysplasia Parkinson disease polycystic kidney disease porphyria porphyria cutanea tarda Rheumatoid arthritis, HLA-DR CIRS ( ...
However, by the end of the decade focus shifted towards patients with Still's disease and juvenile idiopathic arthritis. With ... The Center for Pediatric and Adolescent Rheumatology treats children and adolescents with rheumatic diseases including juvenile ... idiopathic arthritis, but also systemic lupus erythematosus, juvenile dermatomyositis, scleroderma and other connective tissue ...
... and systemic onset juvenile idiopathic arthritis. They have also proven useful for treating cancer, since they are structurally ... HDACi's have been used in various Autoimmune Disorders, such as systemic lupus erythematosus, rheumatoid arthritis, ...
... juvenile idiopathic arthritis, adult and juvenile polymyositis and dermatomyositis, adult and juvenile systemic lupus ... Calcineurin inhibitors are prescribed for adult rheumatoid arthritis (RA) as a single drug or in combination with methotrexate ... It is also prescribed for: psoriatic arthritis, psoriasis, acute ocular Behçet's disease, ...
CYP21B gene and a tenascin TNXB/TNXA-RP2 recombinant between C4A and C4B genes in a patient with juvenile rheumatoid arthritis ...
People with rheumatoid arthritis are less likely to get this, and Drs. Hart and Hooper speculate that this is also true of gout ... In juvenile myoclonic epilepsy (JME), it is a second-line therapy, reserved for when the valproates or lamotrigine do not work ... Broadley, Marissa A. (200). "Juvenile Myoclonic Epilepsy of Janz (JME)". The Childhood Seizure e-Book. Valhalla, New York. ...
Enthesitis Ankylosing spondylitis Juvenile rheumatoid arthritis psoriatic arthritis reactive arthritis Behçet's disease ... Juvenile idiopathic arthritis Sarcoidosis Tubulointerstitial nephritis and uveitis syndrome Systemic disorders that can be ... Rheumatoid arthritis is not uncommon in Asian countries as a significant association of uveitis. Sympathetic ophthalmia Behçet ... Non-neoplastic: retinitis pigmentosa intraocular foreign body juvenile xanthogranuloma retinal detachment Neoplastic: ...
When he was in high school, Robert V. Hine developed severe juvenile rheumatoid arthritis. He was hospitalized for six weeks to ... The hemorrhages were a result of uveitis caused by his rheumatoid arthritis. As he grew older, the uveitis made removal of his ...
Acute exacerbation of juvenile idiopathic arthritis and transient synovitis of the hip both of which are non-septic conditions ... Joints with preexisting arthritis, such as rheumatoid arthritis, are especially prone to bacterial arthritis spread through the ... Acute septic arthritis, infectious arthritis, suppurative arthritis, osteomyelitis, or joint infection is the invasion of a ... Crystal induced arthritis such as gout or pseudogout Inflammatory arthritis Rheumatoid arthritis Seronegative ...
2018). Description of a skull and partial postcranial skeleton of a juvenile elasmosaurid from the Upper Cretaceous Tahora ... Inflammatory arthritis is documented for the first time in snakes, including the aquatic Cretaceous snake Lunaophis aquaticus, ... 2018). An adult specimen of Stereosternum tumidum preserved next to juvenile material, providing new information on the ... Rodrigo A. Otero; José P. O'Gorman; William L. Moisley; Marianna Terezow; Joseph McKee (2018). "A juvenile Tuarangisaurus ...
GWAS studies have shown associations between adult and juvenile bone mass density (BMD) and the Sp7 locus in humans. Though low ... Adiponectin is a protein hormone that has been shown to be upregulated in rheumatoid arthritis disease pathology, causing the ... May 2017). "Response of human rheumatoid arthritis osteoblasts and osteoclasts to adiponectin". Clinical and Experimental ... bone growth by osteoblasts is a partial cause of the abnormal degradation of bone seen in osteoporosis or rheumatoid arthritis ...
and was originally designed for the treatment of chronic myelomonocytic leukemia (CMML) and juvenile myelomonocytic leukemia ( ... lenzilumab was assessed for use in treating inadequately controlled asthma and rheumatoid arthritis. The NIH has chosen ... "Study of KB003 In Biologics-Inadequate Rheumatoid Arthritis" at ClinicalTrials.gov Clinical trial number NCT04583969 at ...
Juveniles and immatures are generally darker and more streaked, with brown to orange eyes and red necks. It closely resembles ... which is used to treat arthritis in cattle, and which lead to kidney failure in vultures who consume carcasses of treated ... The adult is paler than the juvenile, and its underwing coverts can appear almost white at a distance. The head and neck are ...
Persons with dexterity problems, such as with arthritis, may find oral hygiene to be difficult and may require more frequent ... Migliari DA, Sugaya NN, Mimura MA, Cucé LC (1998). "Periodontal aspects of the juvenile form of paracoccidioidomycosis". ...
The model is thought to have suffered from juvenile rheumatoid arthritis. Caravaggio's sleeping Cupid was reconceived in fresco ...
... which some have interpreted as an early depiction of juvenile arthritis or Marfan syndrome. "Portrait of a Youth". National ...
Arthritis and Rheumatism. 62 (3): 791-801. doi:10.1002/art.27305. PMC 2838960. PMID 20187128. Caramés B, Taniguchi N, Seino D, ... "Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism". Nature. 392 (6676): 605-8. Bibcode:1998Natur.392 ... Arthritis and Rheumatism. 64 (4): 1182-92. doi:10.1002/art.33444. PMC 3288456. PMID 22034068. Caramés B, Olmer M, Kiosses WB, ... Arthritis & Rheumatology. 67 (6): 1568-76. doi:10.1002/art.39073. PMC 4446178. PMID 25708836. Furuya, N., Liang, X.H., and ...
The WOMAC has also been used to assess back pain, rheumatoid arthritis, juvenile rheumatoid arthritis, systemic lupus ... A cohort study". Arthritis Care & Research. 65 (1): 15-22. doi:10.1002/acr.21692. PMC 3401342. PMID 22505346. v t e (CS1 maint ... An example of an arthritis study using the WOMAC found a significant exposure-response relationship between body weight loss ( ... Arthritis, Musculoskeletal radiographic signs, Medical scoring system, All stub articles, Medical diagnostic stubs). ...
... juvenile idiopathic arthritis, Still's disease) Keloid morphea Linear atrophoderma of Moulin (Moulin atrophoderma linearis) ... benign juvenile melanoma, epithelioid and spindle cell nevus, Spitz's juvenile melanoma) Solar lentigo (lentigo senilis, liver ... Generalized discoid lupus erythematosus Generalized morphea Interstitial granulomatous dermatitis Juvenile rheumatoid arthritis ... Atlanta, GA: Arthritis Foundation. ISBN 978-0-912423-29-6. Ushiki T (2002). "Collagen fibers, reticular fibers and elastic ...
... especially juvenile rheumatoid arthritis, rheumatoid arthritis, Still's disease, Crohn's disease, ulcerative colitis, ... rheumatoid arthritis Blood cell dysfunction - megaloblastic anemia, myelodysplasia, marrow failure, marrow replacement, acute ... arthritis, systemic lupus erythematosus, Sjögren syndrome, myasthenia gravis, systemic vasculitis, Behcet-like syndrome, ...
Oakford, Glenye Cain (July 10, 2008). "Vindication, juvenile champ and sire, dies at 8". ESPN. Retrieved November 5, 2018. " ... rheumatoid arthritis. Gerald Wiggins, 86, American jazz pianist. Miguel Benavides, 68, Cuban actor. Y. V. Chandrachud, 88, ...
Feng said that she had arthritis and developed pains in her spine, ankles, and wrists due to working on the farm as a teenager ... many who had troubled records and served time in Shanghai's juvenile detention---were sent there. Locals found it challenging ... As a result, many sent-down youth, said Wu, suffered from arthritis when they grew older. Feng Jifang, a female student from ...
Arthritis is caused by inflammation of the joints. Find out all you need to know about juvenile arthritis. ... Overview of Juvenile Idiopathic Arthritis (JIA). Like adults, children can develop arthritis. The most common type of chronic, ... Polyarticular juvenile idiopathic arthritis-rheumatoid factor positive. A child with this type has arthritis in five or more ... Enthesitis-related juvenile idiopathic arthritis. This form of JIA involves both arthritis and enthesitis. Enthesitis happens ...
... is a term used to describe a group of disorders in children that includes arthritis. They are long-term (chronic) diseases that ... Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: ... temporomandibular joint arthritis, and systemic juvenile idiopathic arthritis. Arthritis Care Res (Hoboken). 2022;74(4):521-537 ... Juvenile idiopathic arthritis (JIA) is a term used to describe a group of disorders in children that includes arthritis. They ...
Juvenile arthritis or JA, causes joint swelling, pain, stiffness and loss of motion in children. Learn diagnosis and tests for ... Juvenile Arthritis Also called: Childhood arthritis, JRA, Juvenile idiopathic arthritis, Stills disease ... Juvenile Idiopathic Arthritis (Nemours Foundation) * What Is Juvenile Idiopathic Arthritis (JIA)? (National Institute of ... Oligoarticular Juvenile Idiopathic Arthritis (Nemours Foundation) * Polyarticular Juvenile Idiopathic Arthritis (Nemours ...
Juvenile Rheumatoid Arthritis Learn about the causes, symptoms, diagnosis, and treatment of juvenile rheumatoid arthritis, a ... What is juvenile rheumatoid arthritis? Juvenile rheumatoid arthritis is a disease. It causes joint pain and swelling. It ...
Children with polyarticular juvenile idiopathic arthritis have arthritis in five or more joints during the first 6 months of ... What Is Polyarticular Juvenile Idiopathic Arthritis?. Polyarticular juvenile idiopathic arthritis is a type of juvenile ... Symptoms of Polyarticular Juvenile Idiopathic Arthritis?. Children with polyarticular arthritis may start out with arthritis in ... Children with polyarticular (pol-ee-ar-TIK-yuh-lur) juvenile idiopathic arthritis (polyarticular JIA) have arthritis in five or ...
Adjunctive therapy with curcumin in patients affected by juvenile idiopathic arthritis-associated uveitis improves mild chronic ... Oral phospholipidic curcumin in juvenile idiopathic arthritis-associated uveitis Eur J Ophthalmol. 2020 Nov;30(6):1390-1396. ... Methods: In this retrospective, longitudinal study, we treated patients affected by juvenile idiopathic arthritis-associated ... Conclusion: Adjunctive therapy with curcumin in patients affected by juvenile idiopathic arthritis-associated uveitis improves ...
Access the Radiology study, "Juvenile Idiopathic Arthritis: Diffusion-weighted MRI in the Assessment of Arthritis in the Knee." ... A recent study published in Radiology, "Juvenile Idiopathic Arthritis: Diffusion-weighted MRI in the Assessment of Arthritis in ... Children with juvenile idiopathic arthritis often have autoimmune-mediated inflammation of the synovial membrane. The team ... Diffusion-Weighted MRI Accurate in Detecting Juvenile Idiopathic Arthritis of the Knee. ...
... arthritis ) that first appears before the age of 16. Explore symptoms, inheritance, genetics of this condition. ... Juvenile idiopathic arthritis refers to a group of conditions involving joint inflammation ( ... The most common type of juvenile idiopathic arthritis in the United States is oligoarticular juvenile idiopathic arthritis, ... medlineplus.gov/genetics/condition/juvenile-idiopathic-arthritis/ Juvenile idiopathic arthritis. ...
Most children who have juvenile idiopathic arthritis (JIA) will have some pain and discomfort from the disease. The pain of JIA ... Juvenile Idiopathic Arthritis: Range-of-Motion Exercises * Juvenile Idiopathic Arthritis: Deciding About Total Joint ... Most children who have juvenile idiopathic arthritis (JIA) will have some pain and discomfort from the disease. The pain of JIA ... Quick Tips: Modifying Your Home and Work Area When You Have Arthritis ...
Diseases : Arthritis, Arthritis: Juvenile Chronic, Arthritis: Juvenile Idiopathic, Arthritis: Juvenile Rheumatoid, Ear ... Diseases : Arthritis: Juvenile Idiopathic, Vaccine-induced Toxicity Anti Therapeutic Actions : Vaccination: All, Vaccination: ... 3 Abstracts with Arthritis: Juvenile Idiopathic Research. Filter by Study Type. Human Study. ... Thirty-five percent of children with juvenile idiopathic arthritis experienced flare of the disease after vaccination. Mar 15, ...
... is the most common chronic arthritis of children. It is one of the most common chronic illnesses of childhood and a major cause ... Juvenile idiopathic arthritis (JIA), or juvenile rheumatoid arthritis, is the most common chronic arthritis in children. It is ... Juvenile Idiopathic (Rheumatoid) Arthritis Imaging and Diagnosis * Sections Juvenile Idiopathic (Rheumatoid) Arthritis Imaging ... proposed the term juvenile chronic arthritis (JCA) for the heterogeneous group of disorders that manifest as juvenile arthritis ...
Early juvenile idiopathic arthritis (JIA) is important to recognize as timely diagnosis and treatment improves prognosis. It is ... Validating 10-joint juvenile arthritis disease activity score cut-offs for disease activity levels in non-systemic juvenile ... Early juvenile idiopathic arthritis Katherine Anne B Marzan et al. Rheum Dis Clin North Am. 2012 May. ... Medical treatment of juvenile idiopathic arthritis]. Kröger L, Vähäsalo P, Tynjälä P, Aalto K, Säilä H, Malin M, Putto-Laurila ...
Early juvenile idiopathic arthritis (JIA) is important to recognize as timely diagnosis and treatment improves prognosis. It is ... Validating 10-joint juvenile arthritis disease activity score cut-offs for disease activity levels in non-systemic juvenile ... Early juvenile idiopathic arthritis Katherine Anne B Marzan et al. Rheum Dis Clin North Am. 2012 May. ... Medical treatment of juvenile idiopathic arthritis]. Kröger L, Vähäsalo P, Tynjälä P, Aalto K, Säilä H, Malin M, Putto-Laurila ...
Celiac Disease in Juvenile Idiopathic Arthritis and Other Pediatric Rheumatic Disorders. Journal of Clinical Medicine (2022) * ... Erkan Demirkaya, Dimitri Poddighe, Micol Romano, Kuanysh Dossybayeva, et al.. "Celiac Disease in Juvenile Idiopathic Arthritis ...
Arthritis treatment puts Daanish back in the game When you hear the word arthritis, chances are you think of someone whos ... MCH Steppingstones gives toddlers with arthritis a leg up Toddler Katherine Urquhart was playing at the park when her mother ...
Global HELP provides a free, online medical library with a primary focus on childrens health in underserved communities. Global HELP is a 501(c)(3) nonprofit organization. Click here to find out how you can help us! ...
Juvenile arthritis is the term used for arthritis in children. Arthritis is one category of rheumatic diseases. Rheumatic ... Arthritis is an inflammation of the joints that causes pain and swelling. ... Juvenile arthritis is the term used for arthritis in children. The most common form of juvenile arthritis is juvenile ... Juvenile Arthritis and Other Rheumatic Diseases. What are juvenile arthritis and other rheumatic diseases?. Arthritis is an ...
Juvenile Rheumatoid Arthritis. Michael, Quinn & Connor 2002 USA The basketball game, bicycle ride, and dreams of being a ... Eighteen months after the arm fracture, Conner was diagnosed with juvenile rheumatoid arthritis [JRA]. I remember the shock I ... At this point in the school year, he had already missed the maximum number of school days due to the arthritis pain and chronic ... I ordered the book The New Arthritis Breakthrough and read it cover-to-cover. I also spent many hours on the Internet searching ...
As spontaneous liver involvement in juvenile chronic arthritis is not rare, the possibility of drug induced hepatitis should be ... Two 19 year old patients with juvenile chronic arthritis developed liver toxicity during treatment with sulphasalazine. A ... This is the first report of liver toxicity induced by sulphasalazine in juvenile chronic arthritis. ...
MedlinePlus Genetics related topics: Rheumatoid arthritis Juvenile idiopathic arthritis MedlinePlus related topics: Arthritis ... Arthritis. Arthritis, Rheumatoid. Arthritis, Juvenile. Joint Diseases. Musculoskeletal Diseases. Rheumatic Diseases. Connective ... Safety of Adalimumab in Pediatric Patients with Polyarticular Juvenile Idiopathic Arthritis, Enthesitis-Related Arthritis, ... Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With Juvenile Rheumatoid Arthritis. The safety and ...
One child in every 1,000 in Australia is diagnosed with juvenile arthritis. It is one of the most common chronic conditions to ... Other names for juvenile idiopathic arthritis include juvenile arthritis, juvenile rheumatoid arthritis, juvenile chronic ... What is juvenile idiopathic arthritis?. Juvenile idiopathic arthritis is a group of conditions that cause joint pain and ... Diagnosis of juvenile idiopathic arthritis. Juvenile idiopathic arthritis is diagnosed using a number of tests including:. * ...
Arthritis Cream Osmoflex is a doctor formulated topical analgesic menthol cream that uses a liposomal delivery system to ... Whether you suffer from injury, arthritis, or are looking to protect and improve joint function and mobility, Synotrex can hel ... Category results Arthritis and subcategory Juvenile Arthritis ...
... psoriatic arthritis is sometimes thought of as part of the spectrum of juvenile chronic arthritis, but is now regarded as a ... having more in common with reactive arthritis and juvenile ankylosing spondylitis. ... Juvenile psoriatic arthritis is sometimes thought of as part of the spectrum of juvenile chronic arthritis summarised above but ... Generally, in juvenile chronic arthritis this does not happen but tendons are often inflamed. Of the joints involved the knee ...
Defining criteria for high disease activity in juvenile idiopathic arthritis based on the juvenile arthritis disease activity ... Juvenile idiopathic arthritis (JIA), a group of clinically heterogonous conditions with arthritis of unknown origin beginning ... What are the immunological consequences of long-term use of biological therapies for juvenile idiopathic arthritis? Arthritis ... Rates of hospitalized bacterial infection associated with juvenile idiopathic arthritis and its treatment. Arthritis Rheum. ...
Patients with juvenile idiopathic arthritis (JIA) had lower cardiorespiratory and neuromuscular fitness and were less ... Disease activity was determined by the Juvenile Arthritis Disease Activity score in 10 joints (JADAS-10, score range 0-40). ... Patients With Juvenile Idiopathic Arthritis Less Physically Active Than Controls .social-ris-container { display: flex; justify ... The relationships of kinesiophobia and physical function and physical activity level in juvenile idiopathic arthritis. Pediatr ...
... arthritis), as well as tendon and ligament attachments to... ... Juvenile SpA-ERA constitutes a group of chronic inflammatory ... Juvenile Spondyloarthritis / Enthesitis Related Arthritis (SpA-ERA). Juvenile Spondyloarthritis / Enthesitis Related Arthritis ... Doctors diagnose juvenile SpA-ERA if the onset of the disease is before the age of 16 years, the arthritis lasts for more than ... Juvenile SpA-ERA is one of the most frequent forms of chronic arthritis in childhood and it is more frequently seen in boys ...
Articles tagged with "juvenile idiopathic arthritis (JIA)". 3 AC&R Study Summaries: Treat to Target in Gout, Response to ... Baricitinib Promising for Juvenile Idiopathic Arthritis. July 19, 2022. • By Michele B. Kaufman, PharmD, BCGP ... Case Report: Persistent Knee Warmth Mimics Juvenile Idiopathic Arthritis. March 14, 2022. • By Eman Bamashmous, MBBS, Buthaina ...
... of the self-management program for youth with juvenile idiopathic arthritis (JIA) and their parents to refine the health portal ... for adolescents with arthritis and their parents was developed following a needs assessment. Objective: This study explored the ... Health-related quality of life in adolescents with juvenile idiopathic arthritis. Arthritis Rheum 2006 Apr 15;55(2):199-207 [ ... JIA: juvenile idiopathic arthritis. Edited by G Eysenbach; submitted 08.09.09; peer-reviewed by R Pak, A Joshi; comments to ...
juvenile idiophatic arthritis disease-modifying antirheumatic drugs transition of care smoking DISEASE-ACTIVITY SCORE QUALITY- ... Outcome of transition phase patients with juvenile idiopathic arthritis. Author: Relas, Heikki; Luosujarvi, Riitta; Kosola, ... Outcome of transition phase patients with juvenile idiopathic arthritis. Show full item record ... Relas , H , Luosujarvi , R & Kosola , S 2018 , Outcome of transition phase patients with juvenile idiopathic arthritis , ...
Meningococcal ACWY conjugate vaccine immunogenicity and safety in adolescents with juvenile idiopathic arthritis and ... Meningococcal ACWY conjugate vaccine immunogenicity and safety in adolescents with juvenile idiopathic arthritis and ...
  • The most common type of chronic, or long-lasting, arthritis that affects children is called juvenile idiopathic arthritis (JIA) . (nih.gov)
  • Who Gets Juvenile Idiopathic Arthritis (JIA)? (nih.gov)
  • Oligoarticular juvenile idiopathic arthritis. (nih.gov)
  • Polyarticular juvenile idiopathic arthritis-rheumatoid factor negative. (nih.gov)
  • Polyarticular juvenile idiopathic arthritis-rheumatoid factor positive. (nih.gov)
  • Enthesitis-related juvenile idiopathic arthritis. (nih.gov)
  • Juvenile idiopathic arthritis (JIA) is a term used to describe a group of disorders in children that includes arthritis. (nih.gov)
  • The most common type of JA that children get is juvenile idiopathic arthritis. (medlineplus.gov)
  • Polyarticular juvenile idiopathic arthritis is a type of juvenile idiopathic arthritis (JIA) . (kidshealth.org)
  • Children with polyarticular (pol-ee-ar-TIK-yuh-lur) juvenile idiopathic arthritis (polyarticular JIA) have arthritis in five or more joints during the first 6 months of illness. (kidshealth.org)
  • What Are the Signs & Symptoms of Polyarticular Juvenile Idiopathic Arthritis? (kidshealth.org)
  • How Is Polyarticular Juvenile Idiopathic Arthritis Diagnosed? (kidshealth.org)
  • How Is Polyarticular Juvenile Idiopathic Arthritis Treated? (kidshealth.org)
  • To evaluate the efficacy and the safety of curcumin-phosphatidylcholine complex in children affected by juvenile idiopathic arthritis-associated uveitis as an adjunctive treatment to chronic systemic immunosuppressive therapy. (nih.gov)
  • In this retrospective, longitudinal study, we treated patients affected by juvenile idiopathic arthritis-associated uveitis with residual low-grade inflammatory activity in the anterior chamber with one tablet of curcumin-phosphatidylcholine complex per day, over a year. (nih.gov)
  • Adjunctive therapy with curcumin in patients affected by juvenile idiopathic arthritis-associated uveitis improves mild chronic anterior chamber flare and presents a good safety profile. (nih.gov)
  • Researchers have described seven types of juvenile idiopathic arthritis. (nih.gov)
  • Systemic juvenile idiopathic arthritis causes inflammation in one or more joints. (nih.gov)
  • Oligoarticular juvenile idiopathic arthritis (also known as oligoarthritis) is marked by the occurrence of arthritis in four or fewer joints in the first 6 months of the disease. (nih.gov)
  • Rheumatoid factor positive polyarticular juvenile idiopathic arthritis (also known as polyarthritis, rheumatoid factor positive) causes inflammation in five or more joints within the first 6 months of the disease. (nih.gov)
  • Psoriatic juvenile idiopathic arthritis involves arthritis that usually occurs in combination with a skin disorder called psoriasis . (nih.gov)
  • Enthesitis-related juvenile idiopathic arthritis is characterized by tenderness where the bone meets a tendon, ligament, or other connective tissue. (nih.gov)
  • The last type of juvenile idiopathic arthritis is called undifferentiated arthritis. (nih.gov)
  • This classification is given to affected individuals who do not fit into any of the above types or who fulfill the criteria for more than one type of juvenile idiopathic arthritis. (nih.gov)
  • The incidence of juvenile idiopathic arthritis in North America and Europe is estimated to be 4 to 16 in 10,000 children. (nih.gov)
  • The most common type of juvenile idiopathic arthritis in the United States is oligoarticular juvenile idiopathic arthritis, which accounts for about half of all cases. (nih.gov)
  • For reasons that are unclear, females seem to be affected with juvenile idiopathic arthritis somewhat more frequently than males. (nih.gov)
  • However, in enthesitis-related juvenile idiopathic arthritis males are affected more often than females. (nih.gov)
  • The incidence of juvenile idiopathic arthritis varies across different populations and ethnic groups. (nih.gov)
  • Juvenile idiopathic arthritis is thought to arise from a combination of genetic and environmental factors. (nih.gov)
  • In people with juvenile idiopathic arthritis, the inflammatory response is prolonged, particularly during joint movement. (nih.gov)
  • A recent study published in Radiology , "Juvenile Idiopathic Arthritis: Diffusion-weighted MRI in the Assessment of Arthritis in the Knee," by lead author Anouk Barendregt, MD, in the Department of Pediatric Immunology and Radiology at the Amsterdam University Medical Center, and colleagues, shows MRI technology may make the process of assessing arthritis easier for pediatric patients without sacrificing accuracy. (rsna.org)
  • Diffusion weighted imaging (DWI) is commonly used in areas such as stroke and prostate but has not been widely tested in the diagnosis and analysis of juvenile idiopathic arthritis. (rsna.org)
  • Children with juvenile idiopathic arthritis often have autoimmune-mediated inflammation of the synovial membrane. (rsna.org)
  • Access the Radiology study, " Juvenile Idiopathic Arthritis: Diffusion-weighted MRI in the Assessment of Arthritis in the Knee . (rsna.org)
  • Most children who have juvenile idiopathic arthritis (JIA) will have some pain and discomfort from the disease. (healthlinkbc.ca)
  • Thirty-five percent of children with juvenile idiopathic arthritis experienced flare of the disease after vaccination. (greenmedinfo.com)
  • The microbiota may influence the risk of juvenile idiopathic arthritis and other systemic inflammatory conditions. (greenmedinfo.com)
  • Juvenile idiopathic arthritis (JIA) , or juvenile rheumatoid arthritis, is the most common chronic arthritis in children. (medscape.com)
  • Early juvenile idiopathic arthritis (JIA) is important to recognize as timely diagnosis and treatment improves prognosis. (nih.gov)
  • Ongoing disease activity and changing categories in a long-term nordic cohort study of juvenile idiopathic arthritis. (nih.gov)
  • Early outcomes and improvement of patients with juvenile idiopathic arthritis enrolled in a Canadian multicenter inception cohort. (nih.gov)
  • The most common form of juvenile arthritis is juvenile idiopathic arthritis (JIA). (stanfordchildrens.org)
  • Severe infections are emerging as major risk factors for death among children with juvenile idiopathic arthritis (JIA). (cdc.gov)
  • Juvenile idiopathic arthritis (JIA) is a group of inflammatory joint conditions that affect children and teens under the age of 16. (vic.gov.au)
  • In fact, one in 800 Australian children has a form of juvenile idiopathic arthritis (JIA). (vic.gov.au)
  • It's the least common type of juvenile idiopathic arthritis. (vic.gov.au)
  • This is where the condition does not fit any of the other types of juvenile idiopathic arthritis. (vic.gov.au)
  • As many as 12,000 children in the UK are affected by juvenile idiopathic arthritis (JIA). (papaa.org)
  • Patients with juvenile idiopathic arthritis (JIA) had lower cardiorespiratory and neuromuscular fitness and were less physically active when compared with same aged controls with no JIA diagnosis, according to a study published in Pediatric Rheumatology . (consultantlive.com)
  • Impaired cardiorespiratory and neuromuscular fitness in children and adolescents with juvenile idiopathic arthritis: a cross-sectional case-control study in the era of biologic drug therapies. (consultantlive.com)
  • The relationships of kinesiophobia and physical function and physical activity level in juvenile idiopathic arthritis. (consultantlive.com)
  • This study explored the usability (user performance and satisfaction) of the self-management program for youth with juvenile idiopathic arthritis (JIA) and their parents to refine the health portal prototype. (jmir.org)
  • Juvenile idiopathic arthritis causes joint pain, swelling and stiffness in children under the age of 16. (labiotech.eu)
  • The method involves screening the samples for immunological markers, such as specific types of activated immune cells, and then using machine learning to predict whether the patient has a particular form of juvenile idiopathic arthritis. (labiotech.eu)
  • The algorithm also found some specific markers that were associated with particular types of juvenile idiopathic arthritis. (labiotech.eu)
  • I'm convinced that there will be distinct patterns in the data that will allow us to distinguish between the different types of juvenile idiopathic arthritis, " Wouters explained. (labiotech.eu)
  • Also between juvenile idiopathic arthritis and other types of arthritis that you can have in other immune conditions. (labiotech.eu)
  • Although juvenile idiopathic arthritis is a rare disease , understanding its immunological basis could lead to breakthroughs in more common inflammatory and autoimmune conditions - something that is attracting progressively more corporate interest. (labiotech.eu)
  • Systemic juvenile idiopathic arthritis (sJIA) is a rare, life-threatening inflammatory disease of unknown etiology. (nih.gov)
  • Juvenile idiopathic arthritis is a type of arthritis that affects children and teens. (osmosis.org)
  • The symptoms of juvenile idiopathic arthritis can range from mild to severe, and they may come and go over time. (osmosis.org)
  • Juvenile idiopathic arthritis (JIA) can be difficult for children to live with. (medlineplus.gov)
  • IMSEAR at SEARO: Juvenile idiopathic arthritis: An observational study. (who.int)
  • Juvenile idiopathic arthritis (JIA) has unknown etiology, and the involvement of the temporomandibular joint (TMJ) is rare in the early phase of the disease. (bvsalud.org)
  • 1. Sidiropoulou-Chatzigianni S, Papadopoulos MA, Kolokithas G. Dentoskeletal morphology in children with juvenile idiopathic arthritis compared with healthy children. (bvsalud.org)
  • Treatment of pediatric patients with polyarticular juvenile idiopathic arthritis (pJIA). (nih.gov)
  • Juvenile idiopathic arthritis" is the most common. (nih.gov)
  • Juvenile idiopathic arthritis can affect any joint in the body. (nih.gov)
  • Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications. (nih.gov)
  • IL1RN variation influences both disease susceptibility and response to recombinant human interleukin-1 receptor antagonist therapy in systemic juvenile idiopathic arthritis. (nih.gov)
  • The introduction of biological medication in Juvenile Idiopathic Arthritis (JIA) proposes better therapeutic results with decreased pain and inflammation and consequent reduction in joint damage. (bvsalud.org)
  • Thus, measuring heart rate variability can express autonomous behavior and possibly accompany the response to therapy through the expression of the inflammatory condition Objective Analysis of heart rate variability in a child with Juvenile Idiopathic Arthritis using the anti-Tumor Necrosis Factor. (bvsalud.org)
  • Psoriatic arthritis. (nih.gov)
  • Other features of psoriatic arthritis include abnormalities of the fingers and nails or eye problems. (nih.gov)
  • This helps to diagnose a type of arthritis that involves the skin, such as lupus or psoriatic arthritis. (stanfordchildrens.org)
  • Juvenile psoriatic arthritis (JPsA), accounts for 2 - 15% of new diagnoses and is diagnosed when there is joint pain association with psoriasis. (papaa.org)
  • Juvenile psoriatic arthritis is sometimes thought of as part of the spectrum of juvenile chronic arthritis summarised above but others regard it as a separate disease to be distinguished from these, having more in common with reactive arthritis and juvenile ankylosing spondylitis. (papaa.org)
  • Chronic iridocyclitis , the eye inflammation more usually seen in the form of juvenile chronic arthritis with few joints involved, occurs in 8-17% of cases of psoriatic arthritis of childhood. (papaa.org)
  • Using strict criteria, researchers estimate that psoriatic arthritis accounts for up to 8% of cases of childhood arthritis. (papaa.org)
  • If your child develops painful joints and there is a family history of psoriasis - even if the child shows no psoriasis at the time - it is worth mentioning the possibility to your doctor and even more so, if any family member has psoriatic arthritis. (papaa.org)
  • The main aims of treating juvenile psoriatic arthritis are to reduce joint inflammation, maintain mobility and prevent deformity. (papaa.org)
  • Most children and adolescents with juvenile spondyloarthritis would be diagnosed as affected by ERA and even psoriatic arthritis. (printo.it)
  • It is important that the names "juvenile spondyloarthritis", "enthesitis-related arthritis" and in some cases "psoriatic arthritis" may be the same from a clinical and therapeutic point of view. (printo.it)
  • the clinical features may overlap with each other, including axial and peripheral spondyloarthritis, ankylosing spondylitis, undifferentiated spondyloarthritis, psoriatic arthritis, reactive arthritis and arthritis associated with Crohn's disease and ulcerative colitis. (printo.it)
  • Enthesitis-related arthritis and psoriatic arthritis are two different conditions in the JIA classification and are related to juvenile SpA. (printo.it)
  • Secukinumab in enthesitis-related arthritis and juvenile psoriatic arthritis. (bvsalud.org)
  • It is very rare for more than one member of a family to have JIA, but children with a family member with chronic arthritis, including JIA, are at a slightly increased risk of developing it. (nih.gov)
  • Two 19 year old patients with juvenile chronic arthritis developed liver toxicity during treatment with sulphasalazine. (bmj.com)
  • This is the first report of liver toxicity induced by sulphasalazine in juvenile chronic arthritis. (bmj.com)
  • As spontaneous liver involvement in juvenile chronic arthritis is not rare, the possibility of drug induced hepatitis should be recognised in these patients. (bmj.com)
  • Generally, in juvenile chronic arthritis this does not happen but tendons are often inflamed. (papaa.org)
  • In terms of severity, the condition lies somewhere between the forms of juvenile chronic arthritis with few and with many joints involved. (papaa.org)
  • Juvenile SpA-ERA is one of the most frequent forms of chronic arthritis in childhood and it is more frequently seen in boys than in girls. (printo.it)
  • Depending on the region of the world, it can account for about 30% of children with chronic arthritis. (printo.it)
  • 2. Kjellberg H. Craniofacial growth in juvenile chronic arthritis. (bvsalud.org)
  • 3. Kjellberg H, Fasth A, Kiliaridis S, Wenneberg B, Thilander B. Craniofacial structure in children with juvenile chronic arthritis (JCA) compared with healthy children with ideal or postnormal occlusion. (bvsalud.org)
  • 4. Bakke M, Zak M, Jensen BL, Pedersen FK, Kreiborg S. Orofacial pain, jaw function, and temporomandibular disorders in women with a history of juvenile chronic arthritis or persistent juvenile chronic arthritis. (bvsalud.org)
  • JIA broadly refers to several different chronic disorders involving inflammation of joints (arthritis), which can cause joint pain, swelling, warmth, stiffness, and loss of motion. (nih.gov)
  • This tenderness, known as enthesitis, accompanies the joint inflammation of arthritis. (nih.gov)
  • Enthesitis-related arthritis may also involve inflammation in parts of the body other than the joints. (nih.gov)
  • Arthritis is an inflammation of the joints that causes pain and swelling. (stanfordchildrens.org)
  • A child with this type has arthritis in five or more joints during the first 6 months of the disease. (nih.gov)
  • Arthritis is usually in the hips, knees, ankles, and feet, but the sacroiliac joints (at the base of the back) and spinal joints can also become inflamed. (nih.gov)
  • Children who have arthritis in many joints, or who have fever, rash, and swollen glands may need other medicines. (nih.gov)
  • JIA is a group of disorders that causes arthritis (stiff, swollen, painful joints) in children. (kidshealth.org)
  • Children with polyarticular arthritis may start out with arthritis in only one or two joints, and then increase to more than five. (kidshealth.org)
  • Or they may get arthritis in many joints all at once. (kidshealth.org)
  • If the arthritis is confined to four or fewer joints after 6 months, then the condition is classified as persistent oligoarthritis. (nih.gov)
  • Children with psoriatic JIA have inflammatory arthritis of the joints, and the skin condition psoriasis. (vic.gov.au)
  • Disease activity was determined by the Juvenile Arthritis Disease Activity score in 10 joints (JADAS-10, score range 0-40). (consultantlive.com)
  • A 12-year-old, female, Caucasian patient, with systemic rheumathoid arthritis and involvement of multiple joints was referred to the Imaging Center for TMJ assessment. (bvsalud.org)
  • Arthritis is particularly a problem for children because their bones and joints are developing and growing," says Dr. Michael Ombrello, who specializes in treating joint diseases at NIH. (nih.gov)
  • Other names for this type of arthritis include juvenile spondylitis and juvenile spondyloarthropathies. (vic.gov.au)
  • Learn about the causes, symptoms, diagnosis, and treatment of juvenile rheumatoid arthritis , a joint condition that affects teens and children… What is juvenile rheumatoid arthritis ? (familydoctor.org)
  • A new bilingual (English and French) Internet-based self-management program, Teens Taking Charge: Managing Arthritis Online, for adolescents with arthritis and their parents was developed following a needs assessment. (jmir.org)
  • Like adults, children can develop arthritis. (nih.gov)
  • Diagnosed in children who have arthritis and psoriasis or nail disease, or have a close family member with psoriasis. (nih.gov)
  • Children who have sadness or anger about their arthritis may need extra support . (nih.gov)
  • Some children may continue to have arthritis as adults. (nih.gov)
  • Juvenile arthritis (JA) is arthritis that happens in children. (medlineplus.gov)
  • There are several other forms of arthritis affecting children. (medlineplus.gov)
  • Juvenile arthritis is the term used for arthritis in children. (stanfordchildrens.org)
  • Juvenile arthritis and rheumatic diseases can affect children of any age and any ethnic background. (stanfordchildrens.org)
  • In a proof-of-concept trial, whose results were published in Annals of Rheumatic Diseases , the researchers profiled the immune systems of 85 patients with juvenile arthritis and 43 healthy children. (labiotech.eu)
  • Scientists studying children with juvenile arthritis have found that increased pain and fatigue are linked to reduced participation in school and social activity. (nih.gov)
  • Physicians, conclude the authors, "should consider treating pain more aggressively in children with arthritis with standard pharmacologic therapies. (nih.gov)
  • The two-month study, supported by the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), the Office of Research on Women's Health (ORWH) and the private sector, involved 41 children with juvenile arthritis. (nih.gov)
  • Juvenile arthritis is one of the most prevalent chronic diseases in children in the United States. (nih.gov)
  • While arthritis pain has been the focus of much research in adults, there is an increasing awareness of the need to focus on pain in children. (nih.gov)
  • Children with juvenile arthritis may have pain that can be intense and disabling, and comprehensive treatment optimizes their ability to fully participate in school and social activities. (nih.gov)
  • Schanberg L, Anthony K, Gil K, and Maurin E. Daily pain and symptoms in children with polyarticular arthritis. (nih.gov)
  • A class of drugs called "biologics" has been very helpful for some children with severe arthritis. (nih.gov)
  • This type of arthritis closely resembles rheumatoid arthritis as seen in adults. (nih.gov)
  • Assessing arthritis in the knee can be difficult in adults using traditional MRI methods. (rsna.org)
  • Nearly 1 in 4 adults have had a doctor diagnose them with arthritis, making it one of the main drivers of disability. (cdc.gov)
  • The Centers for Disease Control and Prevention recognizes programs for adults with arthritis to help improve their quality of life. (cdc.gov)
  • Nearly 1 in 3 adults with arthritis and other rheumatic disease report severe joint pain, which can lower quality of life. (cdc.gov)
  • About 10 million adults with arthritis report anxiety or depression symptoms. (cdc.gov)
  • Symptoms of anxiety and depression are common among US adults with arthritis. (cdc.gov)
  • About 15 million US adults with arthritis report severe joint pain, but nearly a third of adults with arthritis are physically inactive. (cdc.gov)
  • Physical activity helps ease severe joint pain for adults with arthritis. (cdc.gov)
  • Joint pain can prevent adults with arthritis from doing everyday activities. (cdc.gov)
  • Exercise helps ease arthritis pain, yet nearly a third of adults with arthritis are physically inactive. (cdc.gov)
  • Treatment of adults with rheumatoid arthritis (RA). (nih.gov)
  • Arthritis is most common in adults. (nih.gov)
  • The study found that DWI was accurate in detecting arthritis in pediatric patients, both in sensitivity and specificity. (rsna.org)
  • DWI also scored above 80% on specificity for patients without arthritis. (rsna.org)
  • What we found in our study quite surprised us - it was better than we expected," said study co-author Robert Hemke, MD, PhD, musculoskeletal radiologist at Amsterdam University Medical Center, who said the team has been researching DWI in arthritis patients for about five years. (rsna.org)
  • With further and larger validation studies, DWI may be valuable for both adult and pediatric arthritis patients, researchers said. (rsna.org)
  • Since a great proportion of patients (up to 85%) with juvenile SpA-ERA are HLA-B27 carriers, the frequency of adult SpA and juvenile SpA-ERA in the general population and even in certain families depends on the frequency of this marker in the normal population. (printo.it)
  • Objectives To assess demography, types of arthritis, treatment modalities and their side effects in patients with arthritis. (who.int)
  • polyarticular onset JIA (20 patients), systemic onset JIA (18 patients), enthesitis related arthritis (13 patients) and pauciarticular onset JIA (10 patients). (who.int)
  • Juvenile arthritis patients and their families recently visited NIAMS to learn about cutting-edge scientific discoveries. (nih.gov)
  • Do you work with patients or clients with arthritis? (cdc.gov)
  • Conduct mental health screenings with your arthritis patients and empower them to take care of both their physical and mental health. (cdc.gov)
  • Ask your arthritis patients about their mental health at their next visit. (cdc.gov)
  • Talk to your arthritis patients about how low-impact exercise can help reduce joint pain. (cdc.gov)
  • Talk to your arthritis patients about incorporating low-impact exercise, like walking and swimming, into their arthritis management plan. (cdc.gov)
  • Talk to your arthritis patients about how exercise can help ease arthritis pain and minimize activity limitations. (cdc.gov)
  • However, it is known that in very few cases the onset of arthritis is preceded by gastrointestinal or urogenital infection (known as reactive arthritis). (printo.it)
  • Some affected individuals develop psoriasis before arthritis while others first develop arthritis. (nih.gov)
  • This form of JIA involves both arthritis and enthesitis. (nih.gov)
  • The rheumatoid factor blood test checks for autoimmune disease, especially rheumatoid arthritis , which is an adult form of arthritis. (nih.gov)
  • It tends to occur in preteen and teenage girls, and it appears to be essentially the same as adult rheumatoid arthritis. (nih.gov)
  • Polyarthritis can be further divided into rheumatoid factor negative arthritis, and rheumatoid factor positive arthritis. (papaa.org)
  • The symptoms your child experiences will depend on the type of arthritis they have. (vic.gov.au)
  • Using artificial intelligence, a Belgian research group can diagnose juvenile arthritis from blood samples with almost 90% accuracy and identify different forms of the disease, something that is not currently possible. (labiotech.eu)
  • To diagnose juvenile arthritis, health care providers perform a physical exam. (nih.gov)
  • There are many types of juvenile arthritis. (nih.gov)
  • Biologics have really changed the face of juvenile arthritis," Ombrello says. (nih.gov)
  • Most people think that arthritis only affects older people. (vic.gov.au)
  • Juvenile SpA-ERA is significantly more common in people that have a positive blood test for the genetic factor HLA-B27. (printo.it)
  • Juvenile SpA-ERA is closely related to the spondyloarthritis with onset in adulthood and most researchers believe these diseases share the same origin and characteristics. (printo.it)
  • A collaboration involving researchers in Belgium and Austria has developed a method to identify which type of juvenile arthritis a patient has based on their blood samples. (labiotech.eu)