AnatomyDiseasesAnalytical, Diagnostic and Therapeutic Techniques and EquipmentAnthropology, Education, Sociology and Social PhenomenaInformation Science
HyperostosisAcquired Hyperostosis SyndromeHyperostosis, Diffuse Idiopathic SkeletalHyperostosis Frontalis InternaHyperostosis, SternocostoclavicularExostosesSyndromeMelorheostosisAnkylosisPaleopathologyPapilloma, InvertedOsteitisHyperostosis, Cortical, CongenitalSpinal OsteophytosisParanasal SinusesSkullCervical VertebraeBone Diseases, DevelopmentalMeningiomaSpinal DiseasesFibulaParanasal Sinus NeoplasmsSternumLongitudinal LigamentsMeningeal NeoplasmsSkull Base NeoplasmsTomography, X-Ray ComputedNose NeoplasmsBone and BonesDown SyndromeThoracic Outlet SyndromeComplex Regional Pain SyndromesCervical Rib SyndromeRibsCervical RibReflex Sympathetic DystrophyEncyclopedias as Topic
Hyperostosis
Increase in the mass of bone per unit volume.
Acquired Hyperostosis Syndrome
Syndrome consisting of SYNOVITIS; ACNE CONGLOBATA; PALMOPLANTAR PUSTULOSIS; HYPEROSTOSIS; and OSTEITIS. The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is indicative of this syndrome.
Hyperostosis, Diffuse Idiopathic Skeletal
A disease of elderly men characterized by large osteophytes that bridge vertebrae and ossification of ligaments and tendon insertions.
Hyperostosis Frontalis Interna
Thickening of the inner table of the frontal bone, which may be associated with hypertrichosis and obesity. It most commonly affects women near menopause.
Hyperostosis, Sternocostoclavicular
A rare, benign rheumatologic disorder or syndrome characterized by hyperostosis and soft tissue ossification between the clavicles and the anterior part of the upper ribs. It is often associated with the dermatologic disorder palmoplantar pustulosis, particularly in Japan. Careful diagnosis is required to distinguish it from psoriatic arthritis, OSTEITIS DEFORMANS, and other diseases. Spondylitis of pustulosis palmaris et plantaris is one of the possible causes; also, evidence suggests one origin may be bone infection. Bone imaging is especially useful for diagnosis. It was originally described by Sonozaki in 1974.
Exostoses
Benign hypertrophy that projects outward from the surface of bone, often containing a cartilaginous component.
Syndrome
A characteristic symptom complex.
Melorheostosis
A form of osteosclerosis extending in a linear track mainly through one of the long bones of the upper and lower limbs.
Ankylosis
Fixation and immobility of a joint.
Paleopathology
The study of disease in prehistoric times as revealed in bones, mummies, and archaeologic artifacts.
Papilloma, Inverted
A mucosal tumor of the urinary bladder or nasal cavity in which proliferating epithelium is invaginated beneath the surface and is more smoothly rounded than in other papillomas. (Stedman, 25th ed)
Osteitis
Inflammation of the bone.
Hyperostosis, Cortical, Congenital
A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed)
Spinal Osteophytosis
Outgrowth of immature bony processes or bone spurs (OSTEOPHYTE) from the VERTEBRAE, reflecting the presence of degenerative disease and calcification. It commonly occurs in cervical and lumbar SPONDYLOSIS.
Paranasal Sinuses
Air-filled spaces located within the bones around the NASAL CAVITY. They are extensions of the nasal cavity and lined by the ciliated NASAL MUCOSA. Each sinus is named for the cranial bone in which it is located, such as the ETHMOID SINUS; the FRONTAL SINUS; the MAXILLARY SINUS; and the SPHENOID SINUS.
Skull
The SKELETON of the HEAD including the FACIAL BONES and the bones enclosing the BRAIN.
Cervical Vertebrae
The first seven VERTEBRAE of the SPINAL COLUMN, which correspond to the VERTEBRAE of the NECK.
Bone Diseases, Developmental
Meningioma
A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7)
Spinal Diseases
Fibula
The bone of the lower leg lateral to and smaller than the tibia. In proportion to its length, it is the most slender of the long bones.
Paranasal Sinus Neoplasms
Tumors or cancer of the PARANASAL SINUSES.
Sternum
A long, narrow, and flat bone commonly known as BREASTBONE occurring in the midsection of the anterior thoracic segment or chest region, which stabilizes the rib cage and serves as the point of origin for several muscles that move the arms, head, and neck.
Longitudinal Ligaments
Two extensive fibrous bands running the length of the vertebral column. The anterior longitudinal ligament (ligamentum longitudinale anterius; lacertus medius) interconnects the anterior surfaces of the vertebral bodies; the posterior longitudinal ligament (ligamentum longitudinale posterius) interconnects the posterior surfaces. The commonest clinical consideration is OSSIFICATION OF POSTERIOR LONGITUDINAL LIGAMENT. (From Stedman, 25th ed)
Meningeal Neoplasms
Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord.
Skull Base Neoplasms
Neoplasms of the base of the skull specifically, differentiated from neoplasms of unspecified sites or bones of the skull (SKULL NEOPLASMS).
Tomography, X-Ray Computed
Tomography using x-ray transmission and a computer algorithm to reconstruct the image.
Nose Neoplasms
Tumors or cancer of the NOSE.
Bone and Bones
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.
Down Syndrome
A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213)
Thoracic Outlet Syndrome
A neurovascular syndrome associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the superior thoracic outlet. This may result from a variety of anomalies such as a CERVICAL RIB, anomalous fascial bands, and abnormalities of the origin or insertion of the anterior or medial scalene muscles. Clinical features may include pain in the shoulder and neck region which radiates into the arm, PARESIS or PARALYSIS of brachial plexus innervated muscles, PARESTHESIA, loss of sensation, reduction of arterial pulses in the affected extremity, ISCHEMIA, and EDEMA. (Adams et al., Principles of Neurology, 6th ed, pp214-5).
Complex Regional Pain Syndromes
Conditions characterized by pain involving an extremity or other body region, HYPERESTHESIA, and localized autonomic dysfunction following injury to soft tissue or nerve. The pain is usually associated with ERYTHEMA; SKIN TEMPERATURE changes, abnormal sudomotor activity (i.e., changes in sweating due to altered sympathetic innervation) or edema. The degree of pain and other manifestations is out of proportion to that expected from the inciting event. Two subtypes of this condition have been described: type I; (REFLEX SYMPATHETIC DYSTROPHY) and type II; (CAUSALGIA). (From Pain 1995 Oct;63(1):127-33)
Cervical Rib Syndrome
A condition associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the thoracic outlet and caused by a complete or incomplete anomalous CERVICAL RIB or fascial band connecting the tip of a cervical rib with the first thoracic rib. Clinical manifestations may include pain in the neck and shoulder which radiates into the upper extremity, PARESIS or PARALYSIS of brachial plexus innervated muscles; sensory loss; PARESTHESIAS; ISCHEMIA; and EDEMA. (Adams et al., Principles of Neurology, 6th ed, p214)
Ribs
A set of twelve curved bones which connect to the vertebral column posteriorly, and terminate anteriorly as costal cartilage. Together, they form a protective cage around the internal thoracic organs.
Cervical Rib
A supernumerary rib developing from an abnormal enlargement of the costal element of the C7 vertebra. This anomaly is found in 1-2% of the population and can put pressure on adjacent structures causing CERVICAL RIB SYNDROME; THORACIC OUTLET SYNDROME; or other conditions.
Reflex Sympathetic Dystrophy
A syndrome characterized by severe burning pain in an extremity accompanied by sudomotor, vasomotor, and trophic changes in bone without an associated specific nerve injury. This condition is most often precipitated by trauma to soft tissue or nerve complexes. The skin over the affected region is usually erythematous and demonstrates hypersensitivity to tactile stimuli and erythema. (Adams et al., Principles of Neurology, 6th ed, p1360; Pain 1995 Oct;63(1):127-33)
Encyclopedias as Topic
Works containing information articles on subjects in every field of knowledge, usually arranged in alphabetical order, or a similar work limited to a special field or subject. (From The ALA Glossary of Library and Information Science, 1983)

SAPHO syndrome of the temporomandibular joint associated with sudden deafness. (1/31)

We report a case of arthritis of the temporomandibular joint (TMJ) associated with sclerosing osteomyelitis of the mandible and temporal bone, causing deafness. The presence of a palmoplantar pustulosis established the diagnosis of SAPHO syndrome. SAPHO (an acronym referring to synovitis, acne, palmoplantar pustulosis, hyperostosis, and osteitis) syndrome is defined by the association of characteristic osteoarticular and dermatologic manifestations, with diffuse sclerosing osteomyelitis of the mandible being a part of this entity. We review the literature of SAPHO syndrome with mandibular manifestations and discuss the mechanisms of inflammatory spread from the TMJ to the cochlea. To our knowledge, this is the first description of skull base involvement in a patient with SAPHO syndrome leading to sudden deafness.  (+info)

SAPHO syndrome or psoriatic arthritis? A familial case study. (2/31)

OBJECTIVE: To discuss the relationships between SAPHO (synovitis, acne, pustulosis, hyperostosis and osteitis) syndrome and the group of spondylarthropathies. METHODS: Few reports of familial SAPHO have been published. We describe three children, two sisters and one brother, whose clinical and radiological presentation was in accordance with SAPHO syndrome. RESULTS: Two children developed psoriasis, and one child palmoplantar pustulosis. Both sacroiliac and sternoclavicular joints were involved in these three cases. Some features in our observations are also common to psoriatic arthritis. No association was found with HLA antigens, but a history of trauma preceding the onset of symptoms was present in all three children. CONCLUSIONS: We can consider that SAPHO is nosologically related to spondylarthropathies. Psoriatic arthritis could be the missing link between SAPHO and spondylarthropathies. It is likely that both genetic and environmental factors are involved.  (+info)

Diagnostic points and possible origin of osteomyelitis in synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome: a radiographic study of 77 mandibular osteomyelitis cases. (3/31)

OBJECTIVES: To find diagnostic points and to identify the origin of osteomyelitis in synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome. METHODS: Fifty-two patients with mandibular suppurative osteomyelitis and 25 patients with mandibular osteomyelitis in SAPHO syndrome were included in the study. Radiographic patterns of the lesion, types of periosteal reaction and the presence of external bone resorption and bone enlargement were investigated in each case and compared between the two entities. RESULTS: Suppurative osteomyelitis demonstrated an osteolytic pattern and a lamellated type of periosteal reaction, whereas SAPHO syndrome revealed a mixed-pattern, solid-type periosteal reaction, external bone resorption and bone enlargement. CONCLUSIONS: Radiographic examination is suggested to be convenient and a useful diagnostic method of differentiating osteomyelitis in SAPHO syndrome from suppurative osteomyelitis. The periosteum is suspected to be the original site of osteomyelitic lesions in SAPHO syndrome.  (+info)

SAPHO syndrome treated with pamidronate: an open-label study of 10 patients. (4/31)

BACKGROUND: In recent years the SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis and osteitis) has been encountered more frequently. However, clinical evidence indicating superiority of a specific therapeutic modality is still absent. Pamidronate, a second-generation bisphosphonate, has a pronounced effect on bone metabolism by suppressing bone resorption. We report our clinical experience with intravenous pamidronate in SAPHO syndrome. METHODS: Between the years 1999 and 2003 we treated 10 patients with the SAPHO syndrome who did not respond to NSAIDs, oral corticosteroids, colchicine, methotrexate, sulphasalazine or infliximab. All patients were treated with 60 mg pamidronate, given intravenously within an hour. In cases of no response a subsequent dose was given within a month and if there was a partial response an additional infusion was given after 4 months. The primary endpoint was the disappearance of recurrent bouts of bone pain, osteitis or hyperostosis, or recurrent synovitis. Reduction of the frequency of attacks by 50% was regarded as a partial response. RESULTS: Seven of the patients were females and three were males. The age at diagnosis ranged from 26 to 68 yr. All patients had axial or peripheral arthritis and cutaneous involvement; three had severe acne, eight had pustulosis and two had concomitant psoriasis vulgaris. Hyperostosis of the anterior chest wall involving either sternocostal or sternoclavicular joints, as seen on technetium 99 bone scintigraphy, was detected in all patients. Complete remission was observed following therapy in six patients, three others partially responded and only one patient had no response. Two patients needed four cycles of pamidronate infusion, one patient needed three, six needed two infusions and one patient remitted following a single pamidronate infusion. In all but one patient pamidronate was effective in preventing recurrent bouts of pustulosis. CONCLUSION: Pamidronate seems to be a very effective mode of therapy for patients with the SAPHO syndrome, by promoting remission in all components of the disorder, such as bone, joint and skin involvement, and ceases the bouts that characterize this disorder.  (+info)

Pamidronate in the treatment of childhood SAPHO syndrome. (5/31)

BACKGROUND: SAPHO syndrome is increasingly recognized within the paediatric population. Conventional therapeutic approaches have often not been effective. Pamidronate is a second-generation bisphosphonate that affects bone turnover and demonstrates anti-inflammatory properties. In small case series it has given symptomatic relief to adults with this condition. OBJECTIVES: To report the clinical experience with pamidronate in childhood SAPHO syndrome. METHODS: A retrospective observational study of all children with SAPHO syndrome treated with pamidronate between 1996 and 2003 at a tertiary rheumatology centre. The standard dosing regime for pamidronate was 1 mg/kg to a maximum of 30 mg, administered daily for three consecutive days, repeated 3-monthly as required. Response to treatment was determined by clinical observation, patient subjective response and reduction in other treatments RESULTS: Seven girls were treated, with a median (range) age at diagnosis of 11 yr (9-15 yr). All patients demonstrated a beneficial clinical response, with relief of pain, increased activity and improved well-being. Subsequent courses of pamidronate were used in all patients. Other medications including corticosteroids and methotrexate could subsequently be stopped. Transient symptoms were associated with the initial course of pamidronate in some patients. No serious adverse events were reported. CONCLUSIONS: Pamidronate was associated with a marked improvement in function and well-being, and a reduction of pain and use of other medications in all patients, with no significant adverse effects. This study represents preliminary clinical data. A prospective multicentre study is necessary to assess the role and long-term safety of pamidronate in the management of childhood SAPHO syndrome  (+info)

Successful treatment of SAPHO syndrome with zoledronic acid. (6/31)

The SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, and osteitis) is a chronic, relapsing, inflammatory condition with skin and osteoarticular manifestations. Its etiology remains unclear, and various treatment regimens with steroids and nonsteroidal antiinflammatory drugs frequently fail to control the disease, while exposing patients to the side effects of these drugs. Because the SAPHO syndrome manifests as a destructive inflammatory bone disease, use of bisphosphonates that possess antiosteoclastic and probably antiinflammatory properties has been suggested to be helpful. To our knowledge, this is the first reported case of successful treatment with zoledronic acid of SAPHO syndrome that was resistant to conventional treatment.  (+info)

Isolated thoracic spine lesion: is this the presentation of a SAPHO syndrome? A case report. (7/31)

A case of an isolated lesion of the thoracic spine attributed to SAPHO syndrome is presented. A 51-year-old man was referred for inflammatory pain in the thoracic spine. The general examination was normal (especially cutaneous and rheumatologic examinations). Laboratory analysis showed only a mild inflammatory reaction. Standard radiographs showed partial condensation of T8. Computed tomography showed osteolysis of the anterior corner of T8, and MRI revealed an abnormal signal of T8, with enlargement of the prevertebral soft tissue. Percutaneous and thoracoscopic biopsies showed a nonspecific inflammatory process, and cultures were sterile. Initially, several diagnoses were advanced: infectious spondylitis, malignant tumor, lymphomas, Paget disease, seronegative spondyloarthropathies and finally atypical SAPHO syndrome. Three months later, the patient experienced more pain. General examination was still normal. The radiological findings worsened, while the inflammatory blood tests were normal. A new thoracoscopic biopsy revealed a nonspecific inflammatory process. A diagnosis of SAPHO syndrome was made, despite the lack of typical lesions. Dramatically improving with anti-inflammatory therapy, the patient's condition was favorable at 3-year follow-up. This atypical presentation of an isolated lesion in the spine makes the diagnosis of a SAPHO syndrome difficult but possible. Spine surgeons must be aware of this rare entity, to avoid misdiagnosis and unnecessary repeated surgical biopsies.  (+info)

The usefulness of bone remodelling markers in predicting the efficacy of pamidronate treatment in SAPHO syndrome. (8/31)

OBJECTIVES: Pamidronate has recently been used in SAPHO syndrome due to its anti-osteoclastic effect. The aim of this study is to determine the usefulness of bone remodelling markers for determining the efficacy of pamidronate treatment. METHODS: Thirteen patients with SAPHO syndrome were treated with pamidronate. The treatment evaluation was done using a visual analogue scale (VAS) and also erythrocyte sedimentation rate, C-reactive protein, serum crosslaps (sCTX) and osteocalcin initially and after 3 months. A relevant clinical response was defined as an improvement in VAS of at least 40%. RESULTS: At 3 months, 7 of 13 patients had a good clinical response, as previously defined. Five of the seven patients maintained the good response over 6 months. Before the first perfusion 6 of the 13 patients had increased sCTX (upper 3250 pmol/l). In this small cohort we tried to analyse whether the increase in bone remodelling markers was associated with a good clinical response. In the responders group the mean levels of sCTX and osteocalcin at baseline were 6783.17 and 24.66, respectively, and in the non-responders group the levels were 2152 and 11.8, respectively. There was a significant difference in sCTX between the responders and the non-responders (P = 0.0044). CONCLUSION: Infusion of pamidronate is effective in SAPHO in some patients. Increased sCTX might be a prognostic marker for a good clinical response but results have to be confirmed in a larger cohort.  (+info)

FRI0243 Sapho syndrome in hungary | Annals of the Rheumatic DiseasesFRI0243 Sapho syndrome in hungary | Annals of the Rheumatic Diseases
Background SAPHO syndrome is an abbreviation according to the suggestion of Chamot (1990) from the words Synovitis, Acne, Pustulosis, Hyperostosis and Osteitis. There are more than 50 synonyms in the first described SAPHO syndrome by Chamot, too. The usage of SAPHO syndrome diagnosis became widespread only in the latest years. ...
http://ard.bmj.com/content/60/Suppl_1/A218.1
Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome: A Case of Spine, Pelvis, and Anterior Chest Wall Involvement,...Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome: A Case of Spine, Pelvis, and Anterior Chest Wall Involvement,...
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is an inflammatory clinical condition with aseptic bone lesions and characteristic skin manifestations. A 63-year-old woman presented with vague musculoskeletal symptoms including chronic buttock pain. The clinical work-up revealed multiple spine and osteoarticular involvement. Multilevel bone marrow edema and cortical erosions involving the spine, asymmetric sacroiliitis, and osteosclerosis of the sternoclavicular joint were consistent with a diagnosis of SAPHO syndrome. Considering SAPHO syndrome in the differential diagnosis, subsequent skin inspection revealed plantar pustulosis. Despite the unique feature of accompanying skin and skeletal lesions, skin lesions could be overlooked if not suspected. ...
https://koreamed.org/article/2016JKSR/2017.76.5.358
SAPHO Syndrome: Get the Facts on Symptoms and CausesSAPHO Syndrome: Get the Facts on Symptoms and Causes
Read about SAPHO syndrome, a disorder involving the skin, bone, and joints. SAPHO is an eponym for the combination of synovitis, acne, pustulosis, hyperostosis, and osteitis. Learn about treatment, symptoms, and diagnosis.
https://www.medicinenet.com/sapho_syndrome/article.htm
SAPHO syndrome | Genetic and Rare Diseases Information Center (GARD) - an NCATS ProgramSAPHO syndrome | Genetic and Rare Diseases Information Center (GARD) - an NCATS Program
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for SAPHO syndrome
https://rarediseases.info.nih.gov/diseases/7606/index
We are currently recruiting patients with Palmoplantar Pustulosis (PPP). This study investigates the Efficacy and safety of...We are currently recruiting patients with Palmoplantar Pustulosis (PPP). This study investigates the Efficacy and safety of...
Clinical trial for Skin Conditions | Skin Infections/Disorders | Psoriasis and Psoriatic Disorders | Dermatology Psoriasis Psoriatic Disorders Palmoplantar Pustulosis , We are currently recruiting patients with Palmoplantar Pustulosis (PPP). This study investigates the Efficacy and safety of ANB019.
https://www.centerwatch.com/clinical-trials/listings/239014/we-are-currently-recruiting-patients-with-palmoplantar-pustulosis-ppp-this-study-investigates-the-efficacy-and-safety-of-anb019/?&geo_lat=45.5369442&geo_lng=-73.5107131&radius=10&place=Longueuil&user_country=Canada&featured=true&rnk=8
ACD A-Z of Skin - Palmoplantar pustulosisACD A-Z of Skin - Palmoplantar pustulosis
Palmoplantar pustulosis (PPP) is a chronic pustular condition affecting the palms of the hands and/or soles of the feet. It may occur with psoriasis or without any other skin disease.
https://www.dermcoll.edu.au/atoz/palmoplantar-pustulosis/
ARAS - What does ARAS stand for? The Free DictionaryARAS - What does ARAS stand for? The Free Dictionary
Looking for online definition of ARAS or what ARAS stands for? ARAS is listed in the Worlds largest and most authoritative dictionary database of abbreviations and acronyms
https://acronyms.thefreedictionary.com/ARAS
How is SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, osteitis) differentiated from hidradenitis suppurativa (HS)?How is SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, osteitis) differentiated from hidradenitis suppurativa (HS)?
The concept of SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, osteitis) includes 4 subgroups of osteoarticular disorders: (1) rheumatologic manifestations associated with acne conglobata o... more
https://www.medscape.com/answers/1073117-30823/1075039-overview
A Placebo-Controlled Double-Blind Study on the Safety and Efficacy of Etanercept in Palmoplantar Pustulosis - Full Text View -...A Placebo-Controlled Double-Blind Study on the Safety and Efficacy of Etanercept in Palmoplantar Pustulosis - Full Text View -...
Palmoplantar pustulosis (PPP) is a chronic recurrent skin condition characterized by the presence of pustules, erythema and hyperkeratosis on palms and soles. PPP can be a severe and disabling disease limiting the ability to walk or work. Although studies on the quality of life of patients with PPP are not available, a recent investigation showed that palmoplantar psoriasis (non pustular) has a more important impact on quality of life than plaque psoriasis. This important impact on quality of life is not surprising as palmoplantar psoriasis as well as palmoplantar pustulosis may limit the ability to work or conduct activities with hands or even impair walking. The disease is sometimes associated with psoriasis elsewhere on the body. Current treatments for PPP include topical corticosteroids, cyclosporine, PUVA therapy, methotrexate and acitretin. Response to topical corticosteroids and PUVA therapy is often disappointing presumably because the thickness of the stratum corneum on palms and soles ...
https://clinicaltrials.gov/show/NCT00353119
Acquired Hyperostosis Syndrome | Profiles RNS
Syndrome consisting of synovitis, acne, palmoplantar pustulosis, hyperostosis, and osteitis (SAPHO). The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is indicative of this syndrome ...
https://profiles.uchicago.edu/profiles/display/31399
Acquired Hyperostosis Syndrome | CTDAcquired Hyperostosis Syndrome | CTD
Syndrome consisting of SYNOVITIS; ACNE CONGLOBATA; PALMOPLANTAR PUSTULOSIS; HYPEROSTOSIS; and OSTEITIS. The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is indicative of this syndrome ...
http://ctdbase.org/detail.go?type=disease&acc=MESH%3AD020083
Patients with palmoplantar pustulosis have increased IL-17 and IL-22 levels both in the lesion and serumPatients with palmoplantar pustulosis have increased IL-17 and IL-22 levels both in the lesion and serum
Recent findings about the pathogenesis of pustulosis palmaris et plantaris (PPP), also known as palmoplantar pustulosis, suggest that IL-17 expression in the acrosyringium as well as infiltration of IL-17 positive cells, e. g. Langerhans cells may play important roles. However, to date, it has not been established whether circulating IL-17 related cytokines are involved in PPP. We studied the circulating IL-17 related cytokines as well as the mRNA levels in lesional skin. IL-17 related cytokine mRNAs were increased in the PPP lesions compared with the control tissues (five patients vs five controls). The serum levels of TNF-alpha, IL-17, IL-22 and IFN-gamma also were significantly increased in PPP, but not IL-23 and IL-8 (48 patients vs 20 controls). Our findings document that not only the serum IL-17 but also tissue IL-17 are elevated in PPP and may be in the pathogenesis of this disorder.. ...
http://uu.diva-portal.org/smash/record.jsf?pid=diva2:448565
SAT0541 Anterior Uveitis in Female Patients: Clinical and Evolutionary Features and Etiological Typification | Annals of the...SAT0541 Anterior Uveitis in Female Patients: Clinical and Evolutionary Features and Etiological Typification | Annals of the...
Results From 698 patients referred, 170 were female with a median age 50,7 years (±17,03) and a median follow-up of 9,05 years (±8). Ocular presentation in 7/170 women had a childhood-onset (,16 years), in 24/170 women had an elderly-onset (≥65 years). Ocular pattern and diagnosis based on age at onset of ocular disease are shown in image 1. 14% patients (24/170) developed another inflammatory ocular affectation. 60,5% patients developed ocular complications. Related to diagnosis highlights macular edema associated with sarcoidosis (33,3%)(p,0.025). Etiological typification: 12% of patients (21/170) had previous rheumatological diagnosis. Adult-onset (12%), elderly-onset (12%),against childhood-onset (43%):7 ankylosing spondylitis (AS)(4%) with median age at diagnosis 40,4 years,2 undifferentiated SpA (1,2%), others (1 multiple sclerosis, 1 ulcerative colitis)(1,2%). 16% of women had SpA as de novo diagnosis: 10 AS, 2 psoriatic SpA, 2 SAPHO syndrome, 2 enteropathic SpA (Crohn, Whipple), 5 ...
http://ard.bmj.com/content/74/Suppl_2/856.1
Most recent papers with the keyword Palmoplantar pustulosis | Read by QxMDMost recent papers with the keyword Palmoplantar pustulosis | Read by QxMD
Pustular psoriasis (PP) is a group of inflammatory skin conditions characterized by infiltration of neutrophil granulocytes in the epidermis to such an extent that clinically visible sterile pustules develop. Because of clinical co-incidence, PP is currently grouped with psoriasis vulgaris (PV). However, PP and PV are phenotypically different, respond differently to treatments and seem to be distinct on the genetic level. In contrast to PV, the phenotypes of PP are not well defined. Descriptions of each form of PP are discordant among standard dermatology textbooks [Saurat Dermatologie 2016, Rooks Dermatology 2016, Fitzpatricks 2012 and Braun-Falco 2012], encumbering the collection of phenotypically well-matched groups of patients as well as clinical trials ...
https://www.readbyqxmd.com/keyword/45448
Keeping it together with an Autoimmune Disease: October 2011Keeping it together with an Autoimmune Disease: October 2011
I tried to get in with their regional(neighborhood) health center, but was told that they dont treat SAPHO so I had to go to main campus to their Rheumatology Institute. My new doctor is wonderful, she is a rheumatology fellow and her mentor is very kind and well accredited rheumy. They got me in in two days, sure beats waiting three months to see my original rheumy ...
http://chronically-inflamed.blogspot.com/2011/10/
Density of Calcium Release Units Decreased, Diffuse Idiopathic Skeletal Hyperostosis, Diminished Respiratory Excursion: Causes ...Density of Calcium Release Units Decreased, Diffuse Idiopathic Skeletal Hyperostosis, Diminished Respiratory Excursion: Causes ...
Density of Calcium Release Units Decreased, Diffuse Idiopathic Skeletal Hyperostosis, Diminished Respiratory Excursion Symptom Checker: Possible causes include Ankylosing Spondylitis, Laryngeal Edema, Asthma. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search.
https://www.symptoma.com/en/ddx/density-of-calcium-release-units-decreased+diffuse-idiopathic-skeletal-hyperostosis+diminished-respiratory-excursion
Diffuse idiopathic skeletal hyperostosis
Diffuse idiopathic skeletal hyperostosis (DISH) is a form of degenerative arthritis characterized by excessive bone growth along the sides of the vertebrae of the spine. Also known as Forestier disease, DISH causes stiffness in the upper back, and may also affect the neck and lower back. Some people experience DISH-associated inflammation and calcification (bone growth) at other areas of the body where tendons and ligaments attach to bone, such as at the heels, ankles, hips, shoulders, elbows, knees and hands. The exact cause of DISH remains unknown, although risk factors such as age, gender, long-term use of certain medications and chronic health conditions have been identified ...
http://diseaseinfosearch.org/Diffuse+idiopathic+skeletal+hyperostosis/9563
Diffuse Idiopathic Skeletal Hyperostosis (DISH): Practice Essentials, Background, PathophysiologyDiffuse Idiopathic Skeletal Hyperostosis (DISH): Practice Essentials, Background, Pathophysiology
Diffuse idiopathic skeletal hyperostosis (DISH) describes a phenomenon characterized by a tendency toward ossification of ligaments. It most characteristically affects the spine.
https://emedicine.medscape.com/article/1258514-overview
chiropractic Care of Diffuse Idiopathic Skeletal Hyperostosis (DISH) | Hutter Chiropractic Officechiropractic Care of Diffuse Idiopathic Skeletal Hyperostosis (DISH) | Hutter Chiropractic Office
Diffuse Idiopathic Skeletal Hyperostosis is the hardening of the spinal ligament where they attach to bone. Gentle care for this condition is available at Hutter Chiropractic Office.
https://www.hutterchiro.com/doctor/chiropractor/chiropractic-Groton/id-your-pain/dish
chiropractic Care of Diffuse Idiopathic Skeletal Hyperostosis (DISH) | Dr. Le's Chiropractic & Wellness, L.L.C.chiropractic Care of Diffuse Idiopathic Skeletal Hyperostosis (DISH) | Dr. Le's Chiropractic & Wellness, L.L.C.
Diffuse Idiopathic Skeletal Hyperostosis is the hardening of the spinal ligament where they attach to bone. Gentle care for this condition is available at Dr. Le's Chiropractic & Wellness, L.L.C..
https://www.chiropracticauburn-al.com/doctor/chiropractor/chiropractic-Auburn/id-your-pain/dish
DISH, Diffuse idiopathic skeletal hyperostosis - BINDEVEVSSYKDOMMER.NOBINDEVEVSSYKDOMMER.NODISH, Diffuse idiopathic skeletal hyperostosis - BINDEVEVSSYKDOMMER.NOBINDEVEVSSYKDOMMER.NO
Diffuse idiopathic skeletal hyperostosis (DISH, Forestiers disease) causes chronic back stiffness in people from 50-60 years of age
https://bindevevssykdommer.no/en/dish-diffus-idiopatisk-skjeletthyperostose/
Pustulosis | definition of pustulosis by Medical dictionaryPustulosis | definition of pustulosis by Medical dictionary
Looking for online definition of pustulosis in the Medical Dictionary? pustulosis explanation free. What is pustulosis? Meaning of pustulosis medical term. What does pustulosis mean?
https://medical-dictionary.thefreedictionary.com/pustulosis
DISH (Diffuse Iliopathic Skeletal Hyperostosis) Sydney, Kogarah & CampbelltownDISH (Diffuse Iliopathic Skeletal Hyperostosis) Sydney, Kogarah & Campbelltown
Spine Service in Campbelltown, Kogarah and Sydney offers treatments for diffuse idiopathic skeletal hyperostosis (DISH). DISH is a condition commonly affecting the spine, characterised by calcification of ligaments, tendons and joint capsule insertions.
https://www.spineservice.com.au/dish-diffuse-iliopathic-skeletal-hyperostosis.html
Psoriasis, Palmo-Plantar Pustulosis occurs in a cyclical pattern, with new pustules occurring after a period of low-to-no...
True drug-induced psoriasis tends to occur in a de-novo fashion in patients with no family or previous history of psoriasis. Practolol is the prototype cardioselective beta blocker, which is no longer available due to the high incidence of cutaneous side effects reported, including psoriasiform eruptions and exacerbations of pre-existing psoriasis. Reports of lithium-provoked psoriasis in the literature include new onset of pustular psoriasis, palmoplantar pustulosis, erythroderma, psoriasiform dermatitis, psoriatic arthropathy, and psoriasis involving the nail and scalp. The refractory period for the development of psoriatic lesions after the initiation of lithium treatment is variable and ranges from a few weeks to several months. It can affect any part of the body, but usually occurs on the scalp, elbows, knees, lower back and genitals, often in the same place on both sides of the body. It can also occur in the fingernails or toenails. Pustular psoriasis is characterized by small pus-filled ...
http://theartchics.com/psoriasis-palmo-plantar-pustulosis-occurs-in-a-cyclical-pattern-with-new-pustules-occurring-after-a-period-of-low-to-no-activity/
Ossification of the Sacrotuberous LigamentsOssification of the Sacrotuberous Ligaments
It has been suggested that ossification of the sacrotuberous ligaments is a good indicator of diffuse idiopathic skeletal hyperostosis (DISH), although others have contested this association. For what its worth, our patient, a 50-year-old man, had no manifestations of DISH in the spine. Ossification of the sacrotuberous ligaments has also been associated with pudendal nerve entrapment ...
http://roentgenrayreader.blogspot.com/2011/12/ossification-of-sacrotuberous-ligaments.html
Search Results from the VAERS DatabaseSearch Results from the VAERS Database
CDC Split Type: Write-up: Pt presents to the ED for c/o L anterior chest wall pain after receiving covid19 vaccination today around 1030. Pt reports she received the first dose in the L bicep. Pt reports after she received that shot she started having L anterior chest wall pain. Pt states she doesnt have any chest tightness but does have stabbing pain to the L anterior chest wall. Pt denies any difficulty breathing or hives or any allergic reaction. Pt was hooked up to cardiac/sp02 and BP monitoring equipment. Medication: Ibuprofen Route: PO Dose:800 mg Patient tolerated medication well; no adverse reaction noted. Medication: Tylenol Route: PO Dose:975 mg Patient tolerated medication well; no adverse reaction noted.. ...
https://www.medalerts.org/vaersdb/findfield.php?EVENTS=on&PAGENO=6&PERPAGE=10&ESORT=&REVERSESORT=&VAX=
Pamidronate (Professional Patient Advice) - Drugs.comPamidronate (Professional Patient Advice) - Drugs.com
Professional guide for Pamidronate. Includes: pharmacology, pharmacokinetics, contraindications, interactions, adverse reactions and more.
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PRIME PubMed | Chronic Recurrent Multifocal Osteomyelitis (CRMO) and Synovitis Acne Pustulosis Hyperostosis Osteitis (SAPHO)...PRIME PubMed | Chronic Recurrent Multifocal Osteomyelitis (CRMO) and Synovitis Acne Pustulosis Hyperostosis Osteitis (SAPHO)...
PubMed journal article Chronic Recurrent Multifocal Osteomyelitis (CRMO) and Synovitis Acne Pustulosis Hyperostosis Osteitis (SAPHO) Syndrome - Two Presentations of the Same Disease? were found in PRIME PubMed. Download Prime PubMed App to iPhone or iPad.
https://www.unboundmedicine.com/medline/citation/30390722/Chronic_Recurrent_Multifocal_Osteomyelitis_
소장자료상세 - 연세대학교 의학도서관소장자료상세 - 연세대학교 의학도서관
History of Acne and Rosacea Acne -- History of Acne and Rosacea Acne -- Acne -- Etiology, Pathophysiology, and Nosology of Acne -- Prevalence -- A Precis of Pathogenesis -- Anatomy of Follicles -- Epidermal Lipids -- Sebaceous Glands -- Micro-organisms -- Endocrinology of Acne -- The Evolution of the Comedo -- Dynamics of Primary Comedo Formation -- Dynamics of Secondary Comedo Formation -- Dynamics of Inflammation -- Inflammatory Lesions and Sequels -- Scope of Scars -- Classification of Acne -- Models of Acne -- Acne in Animals: Canine and Feline Acne -- Animal Models -- Human Sebocyte Cultures -- The Acnes -- Acne in Childhood -- Acne in Puberty and Adulthood -- Acne Comedonica (Comedonal Acne) -- Acne Papulopustulosa (Papulopustular Acne) -- Acne Conglobata -- Acne Inversa -- Acne Fulminans -- SAPHO Syndrome -- Solid Facial Persistent Edema in Acne -- Acne Mechanica -- Back Acne -- Acne Tropicalis (Tropical Acne) -- Postadolescent Acne in Women -- Premenstrual Acne -- Perimenopausal and ...
https://ymlib.yonsei.ac.kr/catalog/search/book-detail/?rurl=%2Fcatalog%2Fsearch%2F%3Fquery%3DMedicine%2B%26Public_Health_%26si%3DTOTAL%26st%3DFRNT%26bk_3%3Djttj2000jttj%26limit%3D10%26bk_1%3Djttjengjttj%26sortkey%3Dpublisher_year%26sortorder%3DDESC%26&cid=CAT000000308547
2boxes=12pcs MiaoLaoDi Magnetic hyperosteogeny plaster, hyperostosis patch orthopetic pain relief plaster Sciatica numbness ...
Immediately your doctor everything this group skeletal, hyperostosis lower click This dictionary contains the following one hundred and - WSU EECS. far fat fax fay fee fen few fey fez fib fie fig fin fir fit fix fly fob foe fog fop for fox fri ...
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SearchSearch
Palmoplantar psoriasis (PP) and palmoplantar pustulosis (PPP) are diseases affecting the hands and/or feet that can cause marked physical discomfort and functional disability. The tumor necrosis factor-alpha antagonists adalimumab, etanercept, and infliximab, the interleukin (IL)-17A inhibitors ixekizumab and secukinumab, and the IL-23 or IL-12/IL-23 inhibitors guselkumab and ustekinumab have been well studied for the treatment of moderate to severe plaque psoriasis. Less is known about the efficacy and safety of these agents for the treatment of PP (hyperkeratotic and pustular forms) and PPP. The aim of this review was to investigate the efficacy of biologic therapy for the treatment of hyperkeratotic PP, pustular PP, and PPP.A systematic search of the medical electronic databases (Medline, Embase, and Cochrane Library) was conducted to identify studies or case reports which both used biologic therapy for the treatment of hyperkeratotic PP, pustular PP, and PPP and reported treatment ...
https://escholarship.org/search/?q=author%3A%22Liao%2C%20Wilson%22
2020 ICD-10-CM Diagnosis Code M48.10: Ankylosing hyperostosis [Forestier], site unspecified2020 ICD-10-CM Diagnosis Code M48.10: Ankylosing hyperostosis [Forestier], site unspecified
Free, official coding info for 2020 ICD-10-CM M48.10 - includes detailed rules, notes, synonyms, ICD-9-CM conversion, index and annotation crosswalks, DRG grouping and more.
https://www.icd10data.com/ICD10CM/Codes/M00-M99/M45-M49/M48-/M48.10
Osteitis | Project Gutenberg Self-Publishing - eBooks | Read eBooks onlineOsteitis | Project Gutenberg Self-Publishing - eBooks | Read eBooks online
Osteitis: | | | Osteitis | | | | Classificati... World Heritage Encyclopedia, the aggregation of the largest online encyclopedias available, and the most definitive collection ever assembled.
http://self.gutenberg.org/articles/eng/Osteitis
Pamidronate Intravenous : Uses, Side Effects, Interactions, Pictures, Warnings & Dosing - WebMDPamidronate Intravenous : Uses, Side Effects, Interactions, Pictures, Warnings & Dosing - WebMD
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Pedal Osteitis...Or Something Else? | The Horse ForumPedal Osteitis...Or Something Else? | The Horse Forum
Recently I acquired a horse that had pretty much come up lame before I got him. The previous owners had the vet take x-rays and the vet diagnosed it as...
https://www.horseforum.com/threads/pedal-osteitis-or-something-else.318234/
Fosamax v. IV Pamidronate - PPMD CommunityFosamax v. IV Pamidronate - PPMD Community
My son, Bobby, is 9 years old and has been on 35mg/weekly of Fosamax for about 2 years. Every 6 months we went back for a DEXA scan and found that while Bobby…
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DermIS - Pustulosis Palmaris et Plantaris (information on the diagnosis)
Acrodermatitis continua, Acrodermatitis continua of Hallopeau, Acrodermatitis perstans, Acrodermatitis perstans continua, Acrodermatitis, continua, Acrodermatitis, continua Hallopeau, Acrodermatitis, perstans, Acropustulosis, Dermatitis repens, Dermatitis, repens, Hallopeaus, acrodermatitis continua, Palmoplantar pust psoriasis, Palmoplantar pustular psoriasis, Palmoplantar pustulosis, Palmoplantaris Pustulosis, PPP - Palmoplantar pustulosis, Pustular acrodermatitis, Pustular Psoriasis of Palms and Soles, Pustular psoriasis of the palms and soles, Pustular psoriasis palms, sole, Pustulosis of Palms and Soles, Pustulosis palmaris et plantar, Pustulosis Palmaris et Plantaris ...
http://dermis.net/dermisroot/en/29338/diagnose.htm
Stress Arthritis Pain Rash Baking Soda --- FELIX-TRAUMLAND UMMLFA
Depression of lactase acitivity in the small intestines of infant rabbits by Candida Plaque Psoriasis of the Elbow The first rung of treatment is topical medications . What Causes Baby Eczema On Face. The nutritional supplements zinc and fish oil appears to improve the skin symptoms. Psoriasis Vulgaris Plaque.. I feel better I do not ache I can think and everyone around me is glad. result when taking methotrexate for psoriasis? I have psoriasis since i was a child. Palmoplantar Pustulosis Palmoplantar pustulosis (PPP) appears on the palms and soles.. Their ebook Cooking Techniques with Olive Oil received a Gold Medal from Dan Poynters Global Ebook Award for Cookbooks. Eczema Flare Up In Breastfed Babies Apple Cider Scalp Vinegar Dermatitis Minnesota Saint Paul While images of psoriasis may seem unsightly to many its important for recognition purpses to see pictures of psoriasis for identification The National Eczema Association says other common Erythrodermic Psoriasis Cure + Guttate Psoriasis ...
http://www.felix-traumland.eu/k5149-stress-arthritis-pain-rash-baking-soda/
Images in rheumatology. Heel enthesopathy of diffuse idiopathi...Images in rheumatology. Heel enthesopathy of diffuse idiopathi...
Images in rheumatology. Heel enthesopathy of diffuse idiopathic skeletal hyperostosis resembling enthesitis of spondyloarthritis.:
https://www.mysciencework.com/publication/show/images-rheumatology-heel-enthesopathy-diffuse-idiopathic-skeletal-hyperostosis-resembling-enthesitis-spondyloarthritis-9f938f5f
Hyperostosis & Narrowing of Medullary Canal & Prognathism: Causes & Reasons - SymptomaHyperostosis & Narrowing of Medullary Canal & Prognathism: Causes & Reasons - Symptoma
Hyperostosis & Narrowing of Medullary Canal & Prognathism Symptom Checker: Possible causes include Van Buchem Disease. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search.
https://www.symptoma.com/en/ddx/hyperostosis+narrowing-of-medullary-canal+prognathism
HKU Scholars Hub: Molecular basis for the increased osteoblast activity in a mouse modelwith hyperostosisHKU Scholars Hub: Molecular basis for the increased osteoblast activity in a mouse modelwith hyperostosis
Cheng, Y. [鄭燕和]. (2005). Molecular basis for the increased osteoblast activity in a mouse model with hyperostosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_ ...
http://hub.hku.hk/handle/10722/29707
Infantile cortical hyperostosis of the mandible<...Infantile cortical hyperostosis of the mandible<...
TY - JOUR. T1 - Infantile cortical hyperostosis of the mandible. AU - Restrepo, Santiago. AU - Sánchez, Ana Maria. AU - Palacios, Enrique. PY - 2004/7/1. Y1 - 2004/7/1. UR - http://www.scopus.com/inward/record.url?scp=3342927640&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=3342927640&partnerID=8YFLogxK. M3 - Article. C2 - 15372912. AN - SCOPUS:3342927640. VL - 83. SP - 454. EP - 455. JO - Ear, Nose and Throat Journal. JF - Ear, Nose and Throat Journal. SN - 0145-5613. IS - 7. ER - ...
https://scholars.uthscsa.edu/en/publications/infantile-cortical-hyperostosis-of-the-mandible
The use of botulinum toxin-A in the management of neck and anterior chest wall flushing: pilot study - Geddoa - 2013 -...The use of botulinum toxin-A in the management of neck and anterior chest wall flushing: pilot study - Geddoa - 2013 -...
Geddoa, E., Matar, H. E. and Paes, T. R. F. (2013), The use of botulinum toxin-A in the management of neck and anterior chest wall flushing: pilot study. International Journal of Dermatology, 52: 1547-1550. doi: 10.1111/ijd.12200 ...
http://onlinelibrary.wiley.com/doi/10.1111/ijd.12200/references?globalMessage=0
Overnight Drugstore: Akismet test viagra money back online!Overnight Drugstore: Akismet test viagra money back online!
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Plus itPlus it
Results. We included 14 patients (women: 10/14; median age at SpA diagnosis: 43.5 yrs, ranging from 19 to 63). Subtypes of SpA were ankylosing spondylitis (n = 11), psoriatic arthritis (n = 2), and synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome (n = 1). HLA-B27 was positive in 3 cases, negative in 9, and unknown in 2. SpA was diagnosed before TA in 13 cases. Imaging findings compatible with the diagnosis of TA were found with computed tomography (11/14) and/or Doppler ultrasound (10/14). Laboratory tests showed increased acute-phase reactants in all cases (C-reactive protein ≥ 25 mg/l in 71% of the cases). All patients except 1 received corticosteroids and 7 were treated with anti-tumor necrosis factor (anti-TNF). ...
http://www.jrheum.org/content/44/7/1011
Welcome to Döbling Osteitis Center - Osteitis Center Döbling, Vienna, AustriaWelcome to Döbling Osteitis Center - Osteitis Center Döbling, Vienna, Austria
In the Osteitis-Center Döbling, 1190 Vienna, all kinds of infections of the skeletal system are treated with the aid of modern equipment.
https://www.osteitiszentrum-doebling.at/en/
Pamidronate Intravenous Advanced Patient Information - Drugs.comPamidronate Intravenous Advanced Patient Information - Drugs.com
Detailed drug Information for pamidronate Intravenous. Includes common brand names, drug descriptions, warnings, side effects and dosing information.
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SPECTRUM Disodium Pamidronate,100mg - 49E365|D3921-100MG - GraingerSPECTRUM Disodium Pamidronate,100mg - 49E365|D3921-100MG - Grainger
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Health & FitnessHealth & Fitness
Did you know the American tobacco companies have a list of 599 additives used to make cigarettes? The big five US cigarette companies (American Tobacco Company, Brown and Williamson, Liggett Group, Inc., Philip Morris Inc. and R.J. Reynolds Tobacco Company) had the list approved by the United States Department of Health and Human Services in 1994. The chemicals used in cigarettes were never tested while burning, and if you listened in science classes at school you would know that burning many of these nasty additives changes their chemical properties, which creates a chemical compound list of 4000 when you burn a cigarette. If this list doesnt make you think about quitting smoking I dont know what will.. ...
http://yxhealth.com/page/2/
Weevil - Encyclopedia of LifeWeevil - Encyclopedia of Life
Definition: A possibly ambiguous term used to describe the presence of the taxon in a region. Common definitions include newly arrived; vagrant; in flux. May or may not have been introduced by human activity ...
https://eol.org/pages/51857759
Thoracic outlet syndromeThoracic outlet syndrome
Rarer acquired causes include tumors (especially pancoast tumor), hyperostosis, and osteomyelitis Adson's sign and the ... Pectoralis minor syndrome May-Thurner syndrome - a similar compressive pathology involving the left common iliac vein Backpack ... Cervical rib syndrome (compression on brachial plexus and/or subclavian artery caused by bone growth). Costoclavicular syndrome ... 100 Operations for Pectoralis Minor Syndrome Alone or Accompanied by Neurogenic Thoracic Outlet Syndrome". Annals of Vascular ...
https://en.wikipedia.org/wiki/Thoracic_outlet_syndrome
List of MeSH codes (C05)List of MeSH codes (C05)
... acquired hyperostosis syndrome MeSH C05.116.099.708.857 - short rib-polydactyly syndrome MeSH C05.116.099.708.914 - ... Klippel-Feil syndrome MeSH C05.116.099.370.652 - orofaciodigital syndromes MeSH C05.116.099.370.797 - Rubinstein-Taybi syndrome ... hyperostosis frontalis interna MeSH C05.116.099.708.582 - Langer-Giedion syndrome MeSH C05.116.099.708.670 - osteochondroma ... Hajdu-Cheney syndrome MeSH C05.116.099.105 - basal-cell nevus syndrome MeSH C05.116.099.343 - dwarfism MeSH C05.116.099.343.110 ...
https://en.wikipedia.org/wiki/List_of_MeSH_codes_(C05)
List of ICD-9 codes 710-739: diseases of the musculoskeletal system and connective tissueList of ICD-9 codes 710-739: diseases of the musculoskeletal system and connective tissue
738 Other acquired deformity 738.0 Acquired deformity of nose 738.1 Other acquired deformity of head 738.2 Acquired deformity ... 710 Diffuse diseases of connective tissue 710.0 Systemic lupus erythematosus 710.2 Sjögren's syndrome 710.3 Dermatomyositis ... myelopathy 721.5 Kissing spine 721.6 Ankylosing vertebral hyperostosis 721.7 Traumatic spondylopathy 722 Intervertebral disc ... acquired) 736.89 Other acquired deformity of other parts of limb Winged scapula 736.9 Acquired deformity, limb, unspec. 737 ...
https://en.wikipedia.org/wiki/List_of_ICD-9_codes_710–739:_diseases_of_the_musculoskeletal_system_and_connective_tissue
Cutibacterium acnesCutibacterium acnes
... hyperostosis, osteitis) syndrome, sarcoidosis and sciatica. It is also suspected a main bacterial source of neuroinflammation ... The antibiotic families that C. acnes are most likely to acquire resistance to are the macrolides (e.g., erythromycin and ...
https://en.wikipedia.org/wiki/Cutibacterium_acnes
List of skin conditionsList of skin conditions
Acquired generalized lipodystrophy (Lawrence syndrome, Lawrence-Seip syndrome) Adiposis dolorosa (Dercum's disease) Alpha-1 ... Rosacea conglobata Synovitis-acne-pustulosis-hyperostosis-osteomyelitis syndrome (SAPHO syndrome) Steroid rosacea Tar acne ... Turner syndrome Ulnar-mammary syndrome Van Der Woude syndrome Von Hippel-Lindau syndrome Watson syndrome Werner syndrome (adult ... Freeman-Sheldon syndrome, Windmill-Vane-Hand syndrome) Wilson-Turner syndrome Wolf-Hirschhorn syndrome (4p- syndrome) X-linked ...
https://en.wikipedia.org/wiki/List_of_skin_conditions
List of diseases (A)List of diseases (A)
Acquired agranulocytosis Acquired central hypoventilation syndrome Acquired hypoprothrombinemia Acquired ichthyosis Acquired ... Ankyloglossia heterochromia clasped thumbs Ankylosing spondylarthritis Ankylosing spondylitis Ankylosing vertebral hyperostosis ... Pande syndrome Aarskog syndrome Aase-Smith syndrome Aase syndrome Abasia ABCD syndrome Abdallat-Davis-Farrage syndrome ... syndrome Akesson syndrome Aksu-Stckhausen syndrome Al Awadi Teebi Farag syndrome Al Frayh Facharzt Haque syndrome Al Gazali Al ...
https://en.wikipedia.org/wiki/List_of_diseases_(A)
List of diseases (D)List of diseases (D)
... chronic spasmodic Dysplasia epiphysealis hemimelica Dysplasia Dysplastic cortical hyperostosis Dysplastic nevus syndrome ... congenital type 3 Dysexecutive syndrome Dysferlinopathy Dysfibrinogenemia, familial Dysfibrinogenemia, acquired Dysgerminoma ... syndrome Daneman-Davy-Mancer syndrome Darier's disease Davenport-Donlan syndrome David syndrome Davis-Lafer syndrome De Barsy ... Salih-Patel syndrome Dinno-Shearer-Weisskopf syndrome Diomedi-Bernardi-Placidi syndrome Dionisi-Vici-Sabetta-Gambarara syndrome ...
https://en.wikipedia.org/wiki/List_of_diseases_(D)
Chiari malformationChiari malformation
... tethered spinal cord syndrome, and connective tissue disorders such as Ehlers-Danlos syndrome and Marfan syndrome. Chiari ... O'Shaughnessy BA, Bendok BR, Parkinson RJ, Shaibani A, Walker MT, Shakir E, Batjer HH (January 2006). "Acquired Chiari ... Congenital causes include hydrocephalus, craniosynostosis (especially of the lambdoid suture), hyperostosis (such as ... Chiari malformation or Arnold-Chiari malformation should not be confused with Budd-Chiari syndrome, a hepatic condition also ...
https://en.wikipedia.org/wiki/Chiari_malformation
List of diseases (H)List of diseases (H)
... homocitrullinuria syndrome Hyperostosid corticalis deformans juvenilis Hyperostosis cortical infantile Hyperostosis corticalis ... acquired Hypertrichosis retinopathy dysmorphism Hypertrichosis, anterior cervical Hypertrichotic osteochondrodysplasia ... Mcdonald syndrome Hunter-Jurenka-Thompson syndrome Hunter-Macpherson syndrome Hunter-Mcalpine syndrome Hunter-Mcdonald syndrome ... child Heavy metal poisoning HEC syndrome Hecht-Scott syndrome Heckenlively syndrome Heide syndrome Heliophobia HELLP syndrome ...
https://en.wikipedia.org/wiki/List_of_diseases_(H)
Joseph MerrickJoseph Merrick
Cohen and Tibbles said Merrick showed the following signs of Proteus syndrome: "macrocephaly; hyperostosis of the large skull; ... there is evidence to suggest that Merrick acquired this particular costume a year later, while travelling with Sam Roper's Fair ... In fact, Proteus syndrome affects tissue other than nerves, and it is a sporadic disorder rather than a genetically transmitted ... In 1986, it was conjectured that he had Proteus syndrome. DNA tests on his hair and bones in a 2003 study were inconclusive ...
https://en.wikipedia.org/wiki/Joseph_Merrick
Norton PrioryNorton Priory
Towards the end of the 14th century, the abbey acquired a "giant" statue of Saint Christopher. Three wills from members of the ... The only major congenital abnormality found consisted of bony changes resulting from a possible case of Down's syndrome. ... Other diseases specific to bones and joints were osteoarthritis, diffuse idiopathic skeletal hyperostosis (DISH), and possible ... and three crania had features of hyperostosis frontalis interna, a metabolic condition affecting post-menopausal women. ...
https://en.wikipedia.org/wiki/Norton_Priory
List of OMIM disorder codesList of OMIM disorder codes
MAT1A Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome; 238970; SLC25A15 Hyperostosis, endosteal; 144750; LRP5 ... acquired; 608709; LMNB2 Lipoid adrenal hyperplasia; 201710; STAR Lipoid congenital adrenal hyperplasia; 201710; CYP11A Lipoid ... AKAP9 Long QT syndrome-3; 603830; SCN5A Long QT syndrome-4; 600919; ANK2 Long QT syndrome-7; 170390; KCNJ2 Long QT syndrome-9; ... TGFBR2 Long QT syndrome 12; 612955; SNT1 Long QT syndrome 13; 613485; KCNJ5 Long QT syndrome-1; 192500; KCNQ1 Long QT syndrome- ...
https://en.wikipedia.org/wiki/List_of_OMIM_disorder_codes
中文中文
Acquired Hyperostosis Syndrome [‎1]‎. Acquired Immunodeficiency Syndrome [‎3043]‎. Acridine Orange [‎1]‎. Acridines [‎1]‎. ...
https://extranet.who.int/iris/restricted/browse?locale-attribute=zh&etal=-1&type=mesh&offset=42&rpp=20&starts_with_previous=A&order=ASC&sort_by=-1
xmlui.Discovery.AbstractSearch.type meshxmlui.Discovery.AbstractSearch.type mesh
Code System ConceptCode System Concept
Myofascial pain syndrome of thorax (disorder) {279036000 , SNOMED-CT } Neoplasm of thorax (disorder) {255058005 , SNOMED-CT } ... Isolated sternocostoclavicular hyperostosis (disorder) {766711009 , SNOMED-CT } Late effect of fracture of thoracic vertebra ( ... Acquired spondylolisthesis of thoracic vertebra (disorder) {321221000119107 , SNOMED-CT } Acute lymphangitis of axilla ( ... Subclavian steal syndrome (disorder) {15258001 , SNOMED-CT } Subclavian vein stenosis (disorder) {234060006 , SNOMED-CT } ...
https://phinvads.cdc.gov/vads/ViewCodeSystemConcept.action?oid=2.16.840.1.113883.6.96&code=118946009
Browsing EMRO RD Speeches and Messages by SubjectBrowsing EMRO RD Speeches and Messages by Subject
Acquired Hyperostosis Syndrome [‎1]‎. Acquired Immunodeficiency Syndrome [‎81]‎. Adolescent Health [‎1]‎. Adolescent Health ...
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Genomics (A-Z)|Home|PHGKBGenomics (A-Z)|Home|PHGKB
Acquired hypoprothrombinemia. *Acquired pure red cell aplasia. *Acquired Von Willebrand syndrome. *Acral dysostosis ... Ankylosing vertebral hyperostosis with tylosis. *Ankylosis of teeth. *Ankyrin-B syndrome. *Annular atrophic lichen planus ... Ameloonychohypohidrotic syndrome. *Amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis and ...
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Code System ConceptCode System Concept
... calvarial hyperostosis syndrome (disorder) {722207000 , SNOMED-CT } Pancreatic triacylglycerol lipase deficiency (disorder) { ... Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome (disorder) { ... Keutel syndrome (disorder) {724208006 , SNOMED-CT } Kostmann syndrome (disorder) {770942003 , SNOMED-CT } Kufor Rakeb syndrome ... Laurence-Moon syndrome (disorder) {232059000 , SNOMED-CT } Leigh syndrome with nephrotic syndrome (disorder) {783157004 , ...
https://phinvads.cdc.gov/vads/ViewCodeSystemConcept.action?oid=2.16.840.1.113883.6.96&code=85995004
Chronic Osteomyelitis Imaging: Practice Essentials, Radiography, Computed TomographyChronic Osteomyelitis Imaging: Practice Essentials, Radiography, Computed Tomography
1] tuberculous osteomyelitis, synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome. [2, 3, 4, 5, 6] ... The images are also relatively poor and may take up to 24 hours to acquire because of the low dosage. ... Characterization of the immune response in the synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) syndrome. ... Vavrík P, Jarošová K, Popelka S, Bek1 J. SAPHO Syndrome - Rare Case of Joint Damage Treated By Knee Synovectomy and Total Hip ...
http://emedicine.medscape.com/article/393345-overview
PesquisarPesquisar
Code System ConceptCode System Concept
Acquired spondylolisthesis of cervical vertebra (disorder) {321151000119106 , SNOMED-CT } Arthropathy of cervical spine facet ... Cervical syndrome (disorder) {111234006 , SNOMED-CT } Closed dislocation cervical spine (disorder) {209037002 , SNOMED-CT } ... Diffuse idiopathic skeletal hyperostosis of cervical spine (disorder) {302311000119107 , SNOMED-CT } Dislocation of ... Branchioskeletogenital syndrome (disorder) {719097002 , SNOMED-CT } Cervical arthritis (disorder) {387801000 , SNOMED-CT } ...
https://phinvads.cdc.gov/vads/ViewCodeSystemConcept.action?oid=2.16.840.1.113883.6.96&code=128049000
Skull Base, Petrous Apex, Tumors Treatment & Management: Medical Therapy, Surgical Therapy, Preoperative DetailsSkull Base, Petrous Apex, Tumors Treatment & Management: Medical Therapy, Surgical Therapy, Preoperative Details
Acquired cholesteatomas are contaminated with bacteria, and great care is required to avoid seeding the subarachnoid space and ... The syndrome of inappropriate antidiuretic hormone secretion (SIADH) and diabetes insipidus (DI) are the most common metabolic ... Hyperostosis of the nearby calvaria can occur. MRI shows broad-based dural attachment, heterogeneous signal pattern, moderately ... Acquired cholesteatomas occur from eustachian tube dysfunction causing retraction of the tympanic membrane or from epithelial ...
https://emedicine.medscape.com/article/883373-treatment
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Acquired Hyperostosis Syndrome (‎1)‎. Acquired Immunodeficiency Syndrome (‎81)‎. Adolescent Health (‎1)‎. Adolescent Health ...
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Acquired Hyperostosis Syndrome (‎1)‎. Acquired Immunodeficiency Syndrome (‎81)‎. Adolescent Health (‎1)‎. Adolescent Health ...
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Browsing EMRO Regional Director by Subject Acquired Hyperostosis SyndromeBrowsing EMRO Regional Director by Subject "Acquired Hyperostosis Syndrome"
Browsing EMRO Regional Director by Subject Acquired Hyperostosis SyndromeBrowsing EMRO Regional Director by Subject "Acquired Hyperostosis Syndrome"
HuGE Navigator|Genopedia|PHGKBHuGE Navigator|Genopedia|PHGKB
University Hospital - Research output - Okayama University
Acquired Hyperostosis Syndrome 100% * Diphosphonates 63% * Osteomyelitis 62% * Mandible 56% * Hyperostosis 9% ... A case of Klippel-Feil and turner syndromes. Park, J. H., Tai, K., Sato, Y., Nishiyama, A. & Shin, J. W., Mar 2012, In: ... A case of chronic lymphocytic leukemia associated with nephrotic syndrome. Mitogawa, T., Nishiya, K., Shikata, K., Makino, H., ... A case of hepatectomy for total situs inversus with Kartagener syndrome. Matsukawa, H., Yagi, T., Sadamori, H., Matsuda, H., ...
https://okayama.pure.elsevier.com/en/organisations/university-hospital/publications/?ordering=title&descending=false&page=3
HuGE Navigator|Phenopedia|PHGKBHuGE Navigator|Phenopedia|PHGKB
Thoracic outlet syndrome - WikipediaThoracic outlet syndrome - Wikipedia
Rarer acquired causes include tumors (especially pancoast tumor), hyperostosis, and osteomyelitis Adsons sign and the ... Pectoralis minor syndrome May-Thurner syndrome - a similar compressive pathology involving the left common iliac vein Backpack ... Cervical rib syndrome (compression on brachial plexus and/or subclavian artery caused by bone growth). Costoclavicular syndrome ... 100 Operations for Pectoralis Minor Syndrome Alone or Accompanied by Neurogenic Thoracic Outlet Syndrome". Annals of Vascular ...
https://en.wikipedia.org/wiki/Thoracic_outlet_syndrome
SAPHO syndrome - Rare Primary Care News
Acquired hyperostosis syndrome; Synovitis, Acne, Pustlosis, Hyperostosis, and Osteomyelitis; Synovitis acne pustulosis ... Visit the following Facebook groups related to SAPHO syndrome:. SAPHO Syndrome Support. Sapho syndrome. SAPHO Syndrome UK ... syndrome. involves any combination of: Synovitis (inflammation of the joints), Acne, Pustulosis (thick yellow blisters ... syndrome. . It can be a chronic condition but sometimes eventually heals on its own. Joint pain may be managed with ...
https://www.rareprimarycarenews.com/rarediseases/sapho-syndrome/
MeSH BrowserMeSH Browser
Acquired Hyperostosis Syndrome [C05.116.099.708.025] * Camurati-Engelmann Syndrome [C05.116.099.708.180] ... Camurati-Engelmann Syndrome Preferred Term Term UI T012013. Date11/11/1974. LexicalTag EPO. ThesaurusID ... Camurati-Engelmann Syndrome Preferred Concept UI. M0006211. Scope Note. An autosomal dominant form of dysplasia that is ... Diaphyseal Hyperostosis Term UI T841055. Date04/18/2013. LexicalTag NON. ThesaurusID GHR (2014). ...
https://meshb.nlm.nih.gov/record/ui?ui=D003966
MeSH BrowserMeSH Browser
Acquired Hyperostosis Syndrome [C05.116.099.708.025] * Camurati-Engelmann Syndrome [C05.116.099.708.180] ... Rare autosomal recessive syndrome characterized by delayed closing of CRANIAL SUTURES, short stature, ACRO-OSTEOLYSIS of distal ... Rare autosomal recessive syndrome characterized by delayed closing of CRANIAL SUTURES, short stature, ACRO-OSTEOLYSIS of distal ...
https://meshb-prev.nlm.nih.gov/record/ui?ui=D058631
Slipped Capital Femoral Epiphyses | Profiles RNS
Acquired Hyperostosis Syndrome. *Camurati-Engelmann Syndrome. *Chondrodysplasia Punctata. *Cleidocranial Dysplasia. *Ellis-Van ...
https://profiles.ouhsc.edu/display/22833
Achondroplasia | Profiles RNS
Silver-Russell Syndrome. *Weill-Marchesani Syndrome. *Osteochondrodysplasias. *Achondroplasia. *Acquired Hyperostosis Syndrome ...
https://profiles.jefferson.edu/display/5905
Diffuse Spinal Hyperostosis Causing Severe Spinal Stenosis and Thoracic Myelopathy | Published in Orthopedic ReviewsDiffuse Spinal Hyperostosis Causing Severe Spinal Stenosis and Thoracic Myelopathy | Published in Orthopedic Reviews
... which demonstrate a unique association between obesity and a novel syndrome of hyperostosis. ... Congenital stenosis is responsible for only 9% of cases with acquired causes including trauma, degenerative changes, iatrogenic ... Diffuse Spinal Hyperostosis Causing Severe Spinal Stenosis and Thoracic Myelopathy. Daniel Alsoof. , George Anderson. , Kevin J ... Kane PM, Daniels AH, Akelman E. Double Crush Syndrome. J Am Acad Orthop Surg. 2015;23(9):558-562. doi:10.5435/jaaos-d-14-00176 ...
https://orthopedicreviews.openmedicalpublishing.org/article/37832
Familial Mediterranean Fever (FMF) Practitioner - Cancer Therapy AdvisorFamilial Mediterranean Fever (FMF) Practitioner - Cancer Therapy Advisor
Muckle-Wells syndrome (MWS), Behcets disease, Crohns disease, Macrophage activation syndrome, Hereditary or acquired ... hyperostosis, osteiitis). ... PFAPA syndrome, TNF receptor associated periodic fever syndrome ... "Pathogenesis of familial periodic fever syndromes or hereditary autoinflammatory syndromes". Am J Physiol Regul Integr Comp ... Systemic autoinflammatory syndromes that share some of these symptoms of FMF. Systemic autoinflammatory syndromes that mimic ...
https://www.cancertherapyadvisor.com/home/decision-support-in-medicine/pediatrics/familial-mediterranean-fever-fmf-practitioner/
Macrocephaly: Background, Pathophysiology, EpidemiologyMacrocephaly: Background, Pathophysiology, Epidemiology
Macrocephaly can be the first manifestation of various congenital and acquired neurologic conditions or may be just a familial ... Neurocutaneous disroders - Tuberous sclerosis, Sturge-weber syndrome, neurofibromatosis, Gorlin syndrome. *Autism spectrum ... Macrocephaly can be the first manifestation of various congenital and acquired neurologic conditions or may be just a familial ... Hyperostosis cranii - associated with disorders such as osteogenesis imperfecta, achondroplasia, and osteopetrosis ...
http://emedicine.medscape.com/article/2500053-overview
Associated Disorders of Chiari Type I MalformationsAssociated Disorders of Chiari Type I Malformations
Other mechanisms exist as well, which can be categorized as either congenital or acquired. In understanding the relationship of ... Shprintzen-Goldberg syndrome. endocrinology. achondroplasia. acromegaly. growth hormone deficiency. hyperostosis. ...
https://www.medscape.com/viewarticle/750325
Pediatrics - OrthopaedicsOne Articles - OrthopaedicsOnePediatrics - OrthopaedicsOne Articles - OrthopaedicsOne
Klippel-Feil syndrome Page: Kyphosis (Pediatric) Page: Legg-Calve-Perthes syndrome Page: Leg length discrepancy (Pediatric) ... Page: Accessory navicular Page: Achondroplasia Page: Acquired flatfoot (Pediatric) Page: Adolescent bunion Page: Adolescent ... Infantile cortical hyperostosis Page: Infantile idiopathic scoliosis Page: Intramembranous bone formation Page: Juvenile ... Downs syndrome Page: Duchenne muscular dystrophy Page: Ehlers-Danlos syndrome Page: Enchondral ossification Page: Ewing ...
https://www.orthopaedicsone.com/display/Main/Pediatrics?atl_token=7cf3e6775544e1931005c3868b8c87a62772d9d4
Pediatrics - OrthopaedicsOne Articles - OrthopaedicsOnePediatrics - OrthopaedicsOne Articles - OrthopaedicsOne
Klippel-Feil syndrome Page: Kyphosis (Pediatric) Page: Legg-Calve-Perthes syndrome Page: Leg length discrepancy (Pediatric) ... Page: Accessory navicular Page: Achondroplasia Page: Acquired flatfoot (Pediatric) Page: Adolescent bunion Page: Adolescent ... Infantile cortical hyperostosis Page: Infantile idiopathic scoliosis Page: Intramembranous bone formation Page: Juvenile ... Downs syndrome Page: Duchenne muscular dystrophy Page: Ehlers-Danlos syndrome Page: Enchondral ossification Page: Ewing ...
https://orthopaedicsone.com/display/Main/Pediatrics?atl_token=c33b511fb8e760bc584d602dbe1a487535de8bd5
Heberdens nodeHeberden's node
Polyarteritis nodosa - Churg-Strauss syndrome - Kawasaki disease - Hypersensitivity vasculitis - Goodpastures syndrome - ... acquired deformities of fingers and toes (Boutonniere deformity, Bunion, Hallux rigidus, Hallux varus, Hammer toe) - other ... Hyperostosis - Osteosclerosis. Osteomyelitis - Avascular necrosis - Pagets disease of bone - Algoneurodystrophy - Osteolysis ... Infantile cortical hyperostosis. Chondropathies. Juvenile osteochondrosis (Legg-Calvé-Perthes syndrome, Osgood-Schlatter ...
https://www.bionity.com/en/encyclopedia/Heberden%27s_node.html
Purchase Paxlovid online - Effective Paxlovid no RX
The shellfish poisoning syndromes are known as paralytic, neurologic, diarrheal, or amnestic depending on the predominant ... Shellfish are occasionally recognized to comprise one or more of several toxins acquired by way of bioaccumulation of sure ... Diffuse idiopathic skeletal hyperostosis. *Carnitine-acylcarnitine translocase deficiency. *Hereditary ataxia. *Hirschsprung ... It should also be averted in any kids with historical past of cardiopulmonary conditions, Down syndrome, at elevated risk for ...
http://www.whalecenter.org/outcomes/purchase-paxlovid-online/
Ankylosing Spondylitis >...Ankylosing Spondylitis >...
Khan MA, Askari AD, Braun WE, Aponte CJ: Low association of HLA‑B27 with Reiters syndrome in Blacks. Ann Intern Med 90: 202‑ ... Diffuse Idiopathic Skeletal Hyperostosis: A Condition That Needs to Be Differentiated from Spondyloarthritis. Curr Rheumatol ... Antonelli M, Bupathi M, Janakiram M, Khan MA. Acquired erythrocytosis on treatment with infliximab for ankylosing spondylitis. ... Khan MA, Braun WE: Acute anterior uveitis in Reiters syndrome: The influence of HLA‑B27 and race. Aust NZ J Med 12: 563‑564, ...
http://spondyloarthritis.com/Publications.aspx
14 Localized Bone Disease | Radiology Key
... hyperostosis, and osteitis). POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes): Solitary ... Late acquired syphilis resembles chronic osteomyelitis. Thickened sclerotic long bones caused by endosteal and periosteal new ... 14.97 Hyperostosis generalisata interna. Irregular thickening of the cranial vault is largely confined to the inner table. Fig ... SAPHO syndrome may be a related condition.. Epidermoid carcinoma occurs in 1% of osteomyelitis at the site of a chronically ...
https://radiologykey.com/14-localized-bone-disease/
Article index A to Z - Character H - Altmeyers EncyclopediaArticle index A to Z - Character H - Altmeyers Encyclopedia
Hyperostosis generalisata with pachydermia Hyperostosis, sterno-costoclavicular Hyperostosis syndrome, acquired (ahs) ...
https://www.altmeyers.org/en/a-bis-z?char=H
Internal Medicine
Synovitis-acne-pustulosis-hyperostosis osteomyelitis (SAPHO) syndrome was diagnosed based on the patients 8-year history of ... Fatal Pulmonary Co-infection with Pneumocystis and Cytomegalovirus in a Patient with Acquired Immunodeficiency Syndrome ... SAPHO syndrome may be associated with skull lesions, which can contribute to the onset of repeated headache or dural thickening ... We herein describe two patients with Brugada syndrome in whom J-waves were successfully modified by drugs. Case 1 was a 54-year ...
https://www.jstage.jst.go.jp/browse/internalmedicine/53/14/_contents/-char/en
Spinal Stenosis Differential Diagnoses
The syndromes of degenerative cervical disease. Orthop Clin North Am. 1992 Jul. 23(3):381-94. [QxMD MEDLINE Link]. ... Quantitative outcome and radiographic comparisons between laminectomy and laminotomy in the treatment of acquired lumbar ... Rheumatologic - Ankylosing spondylitis/spondyloarthropathy, diffuse idiopathic skeletal hyperostosis (DISH). * Infectious - ... Porter RW, Hibbert C, Evans C. The natural history of root entrapment syndrome. Spine (Phila Pa 1976). 1984 May-Jun. 9(4):418- ...
https://www.staging.medscape.com/answers/1913265-75490/what-are-the-differential-diagnoses-for-spinal-stenosis
Spinal Stenosis Differential DiagnosesSpinal Stenosis Differential Diagnoses
The syndromes of degenerative cervical disease. Orthop Clin North Am. 1992 Jul. 23(3):381-94. [QxMD MEDLINE Link]. ... Quantitative outcome and radiographic comparisons between laminectomy and laminotomy in the treatment of acquired lumbar ... Rheumatologic - Ankylosing spondylitis/spondyloarthropathy, diffuse idiopathic skeletal hyperostosis (DISH). * Infectious - ... Porter RW, Hibbert C, Evans C. The natural history of root entrapment syndrome. Spine (Phila Pa 1976). 1984 May-Jun. 9(4):418- ...
https://emedicine.staging.medscape.com/article/1913265-differential
Fluorine and fluorides (EHC 36, 1984)Fluorine and fluorides (EHC 36, 1984)
... yes hyperostosis Moderate gross periosteal no no yes yes hyperostosis Significant incidence of no no no yes lameness Decreased ... NEEDLEMAN, H.L., FUESCHEL, S.M., & ROTHMAN, K.J. (1974) Fluoridation and the occurrence of Downs syndrome. New Engl. J. Med., ... 2. If the fluoridation of drinking-water in an area is discontinued, much of the caries protection acquired by the residents ... No influence of fluoride on the incidence of Downs syndrome was seen. 7.6. Effects on Mortality Patterns Limited evidence is ...
https://inchem.org/documents/ehc/ehc/ehc36.htm
Welcome to PhenoDisWelcome to PhenoDis
Unlike IP, Naegeli syndrome does not evolve through different stages of skin involvement. Naegeli syndrome is extremely rare; ... Caffey disease (infantile hyperostosis; 114000) displays a similar behavior, with pronounced signs suggesting an inflammatory ... any apparent changes in vision or any evidence of acquired strabismus should be evaluated promptly. Head trauma may precipitate ... Because syndrome delineation is fluid, it could be argued that the females with immune regulation abnormalities may not have IP ...
http://mips.helmholtz-muenchen.de/phenodis/disease/show/5666
Fbxl5 Mouse Gene Details | F-box and leucine-rich repeat protein 5 | International Mouse Phenotyping ConsortiumFbxl5 Mouse Gene Details | F-box and leucine-rich repeat protein 5 | International Mouse Phenotyping Consortium
Hypokalemia, Budd-Chiari syndrome, Hyperbilirubinemia, Hypotension, Hypoalbuminemia, Hypercalcemi.... ORPHA:88673. Pura-Related ... Splenomegaly Syndrome With Splenic Germinal Center Hypoplasia And Reduced Circulating T Helper Cells. ...
https://www.mousephenotype.org/data/genes/MGI:2152883
Welcome to Kuwait Pharmacy
Journal of Acquired Immune Deficiency Syndrome?JCV: JC virus?JRA: Juvenile rheumatoid arthritis?JVD: Jugular venous distension? ... Discontinue?DISH: Diffuse idiopathic skeletal hyperostosis?DISIDA: Diisopropyliminodiacetic acid?DIT: diiodotyrosine?div. : ... Acquired Immunodeficiency Syndrome?AIMS: Abnormal involuntary movement scale?AIMS: Alberta Infant Motor Scale?AIP: Acute ... Syndrome of inappropriate antidiuretic hormone?SIB: Self-injurious behavior?SIDS: Sudden infant death syndrome?Sig.: Write on ...
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Code System Concept
Acquired spondylolysis of lumbar spine (disorder) {12071000119102 , SNOMED-CT } Arthropathy of lumbar facet joint (disorder) { ... Diffuse idiopathic skeletal hyperostosis of lumbar spine (disorder) {302331000119102 , SNOMED-CT } Disorder of joint of ... Myofascial pain syndrome of lumbar spine (disorder) {113611000119100 , SNOMED-CT } Neoplasm of lumbar vertebral column ( ... Flatback syndrome of lumbar region (disorder) {308121000119104 , SNOMED-CT } Fracture of lumbar spine (disorder) {125608002 , ...
https://phinvads.cdc.gov/vads/ViewCodeSystemConcept.action?oid=2.16.840.1.113883.6.96&code=129139009
IdiopathicCongenitalInfantileFamilialDiffuseOsteomyelitisDisordersThoracicMacrocephalySAPHOAbnormalitiesDegenerativeBone formationSymptomsGenesImmunodeficiencyDeficiencyAutoimmuneIchthyosisHypermobilityConditionsRareInfectionsPeopleClassical
Idiopathic1
  • Conditions associated with increased risk include psoriasis and Reiter's syndrome, spondyloarthropathy, gout, familial hyperlipidemia, sarcoidosis and diffuse idiopathic skeletal hyperostosis as well as the use of medications such as steroids and fluoroquinolone antibiotics. (doctorputnam.com)
Congenital3
  • Macrocephaly can be the first manifestation of various congenital and acquired neurologic conditions or may be just a familial trait. (medscape.com)
  • It can also be a feature of various congenital syndromes and is then referred to as syndromic macrocephaly. (medscape.com)
  • Other mechanisms exist as well, which can be categorized as either congenital or acquired. (medscape.com)
Infantile1
  • A particular mutation in the COL1A1 gene causes infantile cortical hyperostosis, commonly known as Caffey disease. (medlineplus.gov)
Familial1
  • Familial Mediterranean fever (FMF) is the most common inherited periodic fever syndrome and predominantly affects people of Mediterranean origin. (cancertherapyadvisor.com)
Diffuse4
  • We present three cases of diffuse spinal hyperostosis causing severe spinal stenosis and myelopathy, which demonstrate a unique association between obesity and a novel syndrome of hyperostosis. (openmedicalpublishing.org)
  • This report describes 3 morbidly obese patients with diffuse spinal hyperostosis causing critical thoracic stenosis. (openmedicalpublishing.org)
  • Metabolic changes associated with obesity may result in diffuse hyperostosis with ligament ossification and spinal stenosis. (openmedicalpublishing.org)
  • In this case series, we report a unique association among three cases of critical multilevel spinal stenosis caused by diffuse spinal hyperostosis in young patients with morbid obesity. (openmedicalpublishing.org)
Osteomyelitis1
  • Rarer acquired causes include tumors (especially pancoast tumor), hyperostosis, and osteomyelitis Adson's sign and the costoclavicular maneuver lack specificity and sensitivity and should make up only a small part of the mandatory comprehensive history and physical examination undertaken with a patient suspected of having TOS. (wikipedia.org)
Disorders2
  • Mutations in the COL1A1 gene have been found to cause several forms of Ehlers-Danlos syndrome, a group of disorders that affect the connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. (medlineplus.gov)
  • Capsule?CAPD: Continuous ambulatory peritoneal dialysis?Caps: Capsules?CAPS: Cryopyrin-Associated Periodic Syndromes disorders?CAPTIA Syph G: ?CAPTIA Syph M: ?CAST: Cardiac arrhythmia suppression trials?CAT: Computerized axial tomography?Cataplasm. (kuwaitpharmacy.com)
Thoracic2
  • Thoracic outlet syndrome (TOS) is a condition in which there is compression of the nerves, arteries, or veins in the superior thoracic aperture the passageway from the lower neck to the armpit, also known as the thoracic outlet. (wikipedia.org)
  • The condition was first described in 1818 and the current term "thoracic outlet syndrome" first used in 1956. (wikipedia.org)
Macrocephaly1
SAPHO2
Abnormalities2
  • Rare autosomal recessive syndrome characterized by delayed closing of CRANIAL SUTURES , short stature, ACRO-OSTEOLYSIS of distal phalanges, dental and MAXILLOFACIAL ABNORMALITIES and an increase in bone density that results in frequent BONE FRACTURES . (nih.gov)
  • These changes in collagen increase the risk of blood vessel and organ rupture, and the other abnormalities that can occur with the classical and vascular types of Ehlers-Danlos syndrome. (medlineplus.gov)
Degenerative1
  • The syndromes of degenerative cervical disease. (medscape.com)
Bone formation1
  • This condition is characterized by swelling of soft tissues (muscles, for example), pain, and excessive new bone formation (hyperostosis). (medlineplus.gov)
Symptoms1
  • TOS has similar symptoms to pectoralis minor syndrome (PMS), which usually results from compression of the braxial plexus beneath the pectoralis minor muscle (while neurogenic TOS is caused by compression of the same nerves above the clavicle). (wikipedia.org)
Genes1
  • Ear drops?AutoPap: Computer-assisted cytology interpretation system?AV: Aortic valve?AV: Atrioventricular?A-V: Arteriovenous?AVERT: Atorvastatin Versus Revascularization treatment?AVID: ?AVM: Arteriovenous Malformation?AVNRT: AV nodal reentry tachycardia?AVP: Arginine vasopressin?AVR: Aortic valve replacement?AVR: Augmented V lead, right arm (ECG)?AVRT: ?AVS: Arteriovenous shunt?AWS: Alcohol withdrawal syndrome?AXR: Abdominal X ray?AZF: Azoospermia factor genes?AZT: Azidothymidine (zidovudine)?B & O: Belladonna and opium?B Bx. (kuwaitpharmacy.com)
Immunodeficiency1
  • 1. AIDS: Acquired immune deficiency syndrome Acquired immunodeficiency syndrome 2. (cdc.gov)
Deficiency1
  • The great majority of ichthyoses are inherited, but acquired forms can develop in the setting of malignancy, autoimmune or infectious disease, and nutritional deficiency. (medilib.ir)
Autoimmune1
  • There are many conditions which result in disturbing sleep such as restless leg syndrome, any consistent body pain, myalgic encephalomyelitis, any autoimmune disorder or sleep apnea. (drvikram.com)
Ichthyosis2
  • See "Cutaneous manifestations of internal malignancy", section on 'Acquired ichthyosis' . (medilib.ir)
  • Inherited and acquired forms of ichthyosis have been described, and ocular alterations may occur in specific subtypes. (medscape.com)
Hypermobility1
  • At least five mutations in the COL1A1 gene can result in the arthrochalasia type of Ehlers-Danlos syndrome, which is characterized by an unusually large range of joint movement (hypermobility) and dislocations of both hips at birth. (medlineplus.gov)
Conditions1
  • AIDS-like syndrome: AIDS-like disease (illness) (syndrome) ARC AIDS-related complex Pre-AIDS AIDS-related conditions Prodromal-AIDS 3. (cdc.gov)
Rare1
  • COL1A1 gene mutations are also a very rare cause of the classical and vascular types of Ehlers-Danlos syndrome. (medlineplus.gov)
Infections1
  • The differential prognosis additionally includes different infections such as bacterial pneumonia attributable to neighborhood acquired or atypical organisms, aspiration pneumonia, or pertussis. (whalecenter.org)
People2
  • citation needed] Only 1% of people with carpal tunnel syndrome have concomitant TOS. (wikipedia.org)
  • Additionally, people with classical Ehlers-Danlos syndrome resulting from a COL1A1 gene mutation are prone to tearing (rupture) of major arteries in adulthood. (medlineplus.gov)
Classical1
  • One COL1A1 gene mutation that has been associated with both the classical and vascular types of Ehlers-Danlos syndrome replaces the amino acid arginine with the amino acid cysteine at position 312 in the pro-α1(I) chain (written as Arg312Cys or R312C). (medlineplus.gov)
Browsing EMRO Regional Director by Subject Acquired Hyperostosis Syndrome
Browsing EMRO Regional Director by Subject "Acquired Hyperostosis Syndrome" (apps.who.int)
MeSH Browser
MeSH Browser (meshb-prev.nlm.nih.gov)
Diffuse Spinal Hyperostosis Causing Severe Spinal Stenosis and Thoracic Myelopathy | Published in Orthopedic Reviews
Diffuse Spinal Hyperostosis Causing Severe Spinal Stenosis and Thoracic Myelopathy | Published in Orthopedic Reviews (orthopedicreviews.openmedicalpublishing.org)
(emedicine.medscape.com)
COL1A1 gene: MedlinePlus Genetics
COL1A1 gene: MedlinePlus Genetics (medlineplus.gov)
Spinal Stenosis Differential Diagnoses
Spinal Stenosis Differential Diagnoses (medscape.com)
Chronic Osteomyelitis Imaging: Practice Essentials, Radiography, Computed Tomography
Chronic Osteomyelitis Imaging: Practice Essentials, Radiography, Computed Tomography (emedicine.medscape.com)
(emedicine.medscape.com)
(emedicine.medscape.com)
(emedicine.medscape.com)
(emedicine.medscape.com)
(emedicine.medscape.com)
(emedicine.medscape.com)
(emedicine.medscape.com)
(emedicine.medscape.com)
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
Creator: University of Texas M.D. Anderson Cancer Center - Harold Varmus - Profiles in Science Search Results
Creator: University of Texas M.D. Anderson Cancer Center - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
Creator: UCSF - Harold Varmus - Profiles in Science Search Results
Creator: UCSF - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
Creator: UCSF - Harold Varmus - Profiles in Science Search Results
Creator: UCSF - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
NLMID: 101584930X521 - C. Everett Koop - Profiles in Science Search Results
NLMID: 101584930X521 - C. Everett Koop - Profiles in Science Search Results (profiles.nlm.nih.gov)
NLMID: 101584926X184 - Harold Varmus - Profiles in Science Search Results
NLMID: 101584926X184 - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results
Exhibit Tags: aids - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)
Creator: UCSF - Harold Varmus - Profiles in Science Search Results
Creator: UCSF - Harold Varmus - Profiles in Science Search Results (profiles.nlm.nih.gov)