... and long-term exposure results in kidney failure and bone problems. Heart disease, hypertension, and lung cancer are other ... Thailand: In Thailand, e-waste can also lead to human health risks, such as cancer and human developmental difficulties, if it ... High levels of dioxin compounds, which are linked to cancer and developmental defects, have been commonly found in the breast ... In Guiyu, 80% of the children suffer from respiratory diseases because children typically work in or live near waste disposal ...

... foamy histiocytes in bone marrow; visceral mucopolysaccharide storage similar to that in Hurler disease; GM1 storage in ... This subtype is characterized by a trajectory in which some developmental skills are gained, then they stabilize and delays ... Lyon G, Adams RD, Kolodny EH (1996). Neurology of Hereditary Metabolic Diseases of Children (2nd ed.). New York: McGraw-Hill, ... July 2011). "GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings". Biochimica et ...

Veilleux LN, Rauch F (October 2017). "Muscle-Bone Interactions in Pediatric Bone Diseases". Current Osteoporosis Reports. 15 (5 ... Pediatric and Adult Nutrition in Chronic Diseases, Developmental Disabilities, and Hereditary Metabolic Disorders: Prevention, ... People with cerebral palsy are at risk of low bone mineral density. The shafts of the bones are often thin (gracile), and ... In cerebral palsy unequal growth between muscle-tendon units and bone eventually leads to bone and joint deformities. At first ...

... relapse of malignant disease and incidence of acute and chronic graft-versus-host diseases if they are used for prophylactic ... A bone marrow biopsy provides conclusive proof of ALL, typically with >20% of all cells being leukemic lymphoblasts. A lumbar ... Recent studies showed that CNS chemotherapy provided results as favorable but with fewer developmental side effects. As a ... Cytogenetic testing on the marrow samples can help classify disease and predict how aggressive the disease course will be. ...

Juvenile veiled chameleons in captivity often develop nutritional metabolic bone disease but will not develop it if fed dietary ... This makes them an excellent model organism to study developmental and evolutionary phenomena. Young chameleons have a ... Odontoblasts produce a layer of predentin that connects the dentine to the supporting bone with both tooth and bone protruding ... "Nutritional Metabolic Bone Disease in Juvenile Veiled Chameleons (Chamaeleo calyptratus) and Its Prevention". The Journal of ...

ISSD is the most severe form of the sialic acid storage diseases. Babies with this condition have severe developmental delay, ... bone malformations, enlarged liver and spleen (hepatosplenomegaly), and an enlarged heart (cardiomegaly). Approximately ~250 ... Infantile free sialic acid storage disease (ISSD) is a lysosomal storage disease. ISSD occurs when sialic acid is unable to be ... Individuals with FSASD may go misdiagnosed or undiagnosed, making it difficult to determine the true frequency of the disease ...

Brittle Bone Disorders Consortium (BBD), Brendan Lee, M.D., Ph.D., Baylor College of Medicine, Houston, TX. Clinical Research ... Developmental Synaptopathies Consortium (DSC), Mustafa Sahin, M.D., Ph.D., Boston Children's Hospital, Boston, MA. Dystonia ... The Rare Diseases Clinical Research Network (RDCRN) is an initiative of the US Office of Rare Diseases Research (ORDR). RDCRN ... The following is a timeline of the Rare Diseases Clinical Research Network: As a result of the Rare Diseases Act of 2002, on ...

... chronic kidney disease, cranio-facial dysmorphisms, hypoplasia of the iliac bones, lupus nephritis, arthralgia, arthritis, ... Rare symptoms include intellectual disability, developmental delay, progressive spastic quadriplegia, temporomandibular joint ... Silve C, Jüppner H (September 2006). "Ollier disease". Orphanet Journal of Rare Diseases. 1 (1): 37. doi:10.1186/1750-1172-1-37 ... "Spondyloenchondrodysplasia with immune dysregulation - About the Disease - Genetic and Rare Diseases Information Center". ...

December 2019). "Single-cell analysis of bone marrow-derived CD34+ cells from children with sickle cell disease and thalassemia ... Developmental changes and kinetic alterations". Annals of the New York Academy of Sciences. 938 (1): 139-145. Bibcode:2001NYASA ... Cells expressing CD34 (CD34+ cell) are normally found in the umbilical cord and bone marrow as haematopoietic cells, or in ... It may also mediate the attachment of hematopoietic stem cells to bone marrow extracellular matrix or directly to stromal cells ...

"Allogeneic bone marrow transplantation for Alexander's disease". Bone Marrow Transplant. 20 (3): 247-9. doi:10.1038/sj.bmt. ... Symptoms include mental and physical developmental delays, followed by the loss of developmental milestones, an abnormal ... alexander_disease at NINDS "Cause of brain disease found". January 2, 2001 - via news.bbc.co.uk. "Alexander Disease - United ... Wikimedia Commons has media related to Alexander disease. OMIM entries on Alexander disease Infantile-onset Alexander disease ...

Developmental delay hypotonia extremities hypertrophy Developmental dyslexia Developmental dysphasia familial Devic syndrome ... induced lung disease Dwarfism Dwarfism bluish sclerae Dwarfism deafness retinitis pigmentosa Dwarfism lethal type advanced bone ... This is a list of diseases starting with the letter "D". Diseases Alphabetical list 0-9 A B C D E F G H I J K L M N O P Q R S T ... myopathy Desmoid disease Desmoid tumor Desmoplastic small round cell tumor Developmental coordination disorder Developmental ...

Other signs can include multiple mostly noncancerous benign bone tumours called osteochondromas (exostosis), developmental ... It is classified as a rare disease. The signs and symptoms of Potocki-Shaffer syndrome vary widely. In addition to multiple ... The disorder is associated with an enlarged parietal foramina which can cause openings in the two bones that form the top and ... OMIM entry Genetic & Rare Diseases Information Center entry Archived 2012-09-19 at the Wayback Machine Genetics Home Reference ...

Holt-Oram syndrome can cause a hole in the septum, bone abnormalities in the fingers, wrists, or arms, and a conduction disease ... Mutations in this gene can result in Holt-Oram syndrome, a developmental disorder affecting the heart and upper limbs. ... Boogerd CJ, Evans SM (February 2016). "TBX5 and NuRD Divide the Heart". Developmental Cell. 36 (3): 242-244. doi:10.1016/j. ... T-box genes encode transcription factors involved in the regulation of developmental processes. This gene is closely linked[ ...

The Human Developmental Anatomy Center maintains the largest collection of embryologic material in the United States. The ... But new weapons and new environments bring new injuries, and epidemic disease remains a foe uniting all eras of combat. The ... The Anatomical Collections are made up of bones and body parts. More than 5,000 skeletal specimens and 10,000 preserved organs ... "National Museum of Health and Medicine (NMHM): Human Developmental Anatomy Center". Medicalmuseum.mil. Retrieved 2019-06-19. " ...

Otologist Physician/surgeon who specializes in diseases of the ear. Otosclerosis Abnormal growth of bone of the inner ear. This ... Developmental verbal dyspraxia In individuals with normal muscle tone and speech muscle coordination, partial loss of the ... Ulna Long bone in the arm on the pinky side that goes from the humerus to the carpal. Velocardiofacial syndrome Inherited ... Glaucoma Disease related to eyes due to increase in IOP(intraorbicular pressure) Hair cells Sensory cells of the inner ear, ...

... such as facial bone fractures and breaks; congenital abnormalities, such as cleft palates or cleft lips; developmental ... Hand surgery is concerned with acute injuries and chronic diseases of the hand and wrist, correction of congenital ... Free flaps of skin, muscle, bone, fat, or a combination may be removed from the body, moved to another site on the body, and ... It is also commonly used in patients with Arthritis as it acts like a cushion to the bones which have depleted the articular ...

Whyte MP (September 2017). "Hypophosphatasia: An overview For 2017". Bone. Rare Bone Diseases. 102: 15-25. doi:10.1016/j.bone. ... Taillefer D. "Our Mission". Soft Bones Canada Inc. Rathbun JC (June 1948). "Hypophosphatasia; a new developmental anomaly". ... DXA may show abnormal bone mineral density which may correlate with disease severity, although bone mineral density in HPP ... or ALP-rich serum from patients with Paget's bone disease, was not beneficial. Phase 2 clinical trials of bone targeted enzyme- ...

... as well as expressed in 76 developmental stages. C8orf48 has been found to be expressed most often in the bladder, bone, heart ... regarding multiple myeloma bone marrow mesenchymal stromal cells shows that the expression of C8orf48 is lower in the disease ... In regards to the developmental stages, C8orf48 was most often found in the embroid body. In a study ... it was found that C8orf48 levels are higher in the disease state than in the healthy state. Other studies demonstrate ...

... and Paget's disease of bone. A dilaceration is a bend in the root which may have been caused by trauma to the tooth during ... Developmental abnormalities most commonly affect the number, size, shape, and structure of teeth. Tooth abnormalities caused by ... The alveolar bone is the bone of the jaw which forms the alveolus around teeth. Like any other bone in the human body, alveolar ... The disease can lead to pain, tooth loss, and infection. Dental caries has a long history, with evidence showing the disease ...

Gingival diseases - non dental biofilm induced Genetic/developmental disorders Specific infections Inflammatory and immune ... Radiographs such as bitewings, intra-oral periapicals or a panoramic radiograph can be taken to help assess the bone loss and ... Classification of Periodontal Diseases 2018 In 2018, a new classification system for Periodontal diseases was released. It has ... Necrotizing periodontal diseases II) Periodontitis III) Periodontitis as a manifestation of systemic disease In the third ...

The disease consists of a chronic inflammation associated with loss of alveolar bone. Advanced disease features include pus and ... The presence of certain developmental or acquired conditions can influence the outcome of periodontitis (see table). Plaque- ... Rather than a single disease entity, periodontal disease is a combination of multiple disease processes that share a common ... Periodontal pathology, also termed gum diseases or periodontal diseases, are diseases involving the periodontium (the tooth ...

Paleopathology is the study of disease in antiquity. This study focuses not only on pathogenic conditions observable in bones ... developmental, genetic) to environmental stresses. Human biology is an interdisciplinary field of biology, biological ... Lewin, Roger (1997). Bones of contention : controversies in the search for human origins (2nd ed., with a new afterword ed.). ... The examined human remains usually are limited to bones but may include preserved soft tissue. Researchers in bioarchaeology ...

Mixed connective tissue disease Mixed Müllerian tumor Mixed receptive-expressive language disorder Mixed sclerosing bone ... MIDAS syndrome Midline cleft of lower lip Midline defects autosomal type Midline defects recessive type Midline developmental ... This is a list of diseases starting with the letter "M". Diseases Alphabetical list 0-9 A B C D E F G H I J K L M N O P Q R S T ... Mitochondrial diseases of nuclear origin Mitochondrial diseases, clinically undefinite Mitochondrial disease Mitochondrial ...

2007: Nick Hales Award for outstanding contribution to the developmental origins of health and disease. "Karen A Lillycrop". ... Childhood bone mineral content is associated with methylation status of the RXRA promoter at birth. Journal of Bone and Mineral ... Epigenetic mechanisms in the developmental origins of adult disease. Roach, Helmtrud I., Bronner, Felix and Oreffo, Richard O.C ... an international consortium which investigates the role of epigenetic processes in the developmental origins of disease. 2014 ...

Joan Mondale, 83, American arts advocate, Second Lady of the United States (1977-1981), Alzheimer's disease. Helmut Niedermeyer ... Richard Daugherty, 91, American archaeologist, led excavation of Ozette Indian Village, bone cancer. Charlotte Dawson, 47, New ... K. Alison Clarke-Stewart, 70, Canadian developmental psychologist. G. Bhuvaraghan, 86, Indian politician, MP for Cuddalore ( ... Rose Finn-Kelcey, 68, British artist, motor neurone disease. Seyed Kazem Ghiyassian, 74, Iranian footballer (Aboumoslem, Payam ...

For example, females are often seen to be at a higher risk of bone fracture due to osteoporosis. Although females do lose bone ... Females also report a higher prevalence of many pain-related diseases and syndromes, particularly auto-immune diseases. In a ... Males are more likely to suffer from alcoholism and antisocial personality disorder, as well as developmental psychiatric ... Exercise and activity in childhood help to build up higher density bones. Although in Britain female's bones are less dense ...

... of the molecular biology of bones and teeth section in the MTB which subsequently became the craniofacial and skeletal diseases ... She earned a Ph.D. in developmental biology from the University of Connecticut in the department of genetics and cell biology. ... As of 2018, Young was a senior investigator and chief of the molecular biology of bones and teeth section. In August 2018, she ... The group also investigates how stem cell fate can be regulated by the ECM in multiple skeletal sites including bones, teeth, ...

... impairments caused by disease (e.g., poliomyelitis, bone tuberculosis), and impairments from other causes (e.g., cerebral palsy ... This is compared to 63.9% of students with a developmental delay or 47% with emotional disturbance. According to IDEA, deaf- ... According to IDEA, an individual with autism is someone with "a developmental disability significantly affecting verbal and ... the combination of which causes such severe communication and other developmental and educational needs that they cannot be ...

mild to moderate to severe intellectual disability, also called "developmental disability" short fifth digits with hypoplastic ... and thick eyebrows and lashes Disease can be inherited as an autosomal dominant trait, however most cases of CSS appear to be ... birth weight feeding difficulties upon birth frequent respiratory infections during infancy hypotonia joint laxity delayed bone ... is a rare genetic disorder that causes developmental delays and absent fifth finger and toe nails. There had been 31 reported ...

Medial eyebrow flare Low nasal bridge Low-set large ears Osteogenesis imperfecta Widespread developmental delay Wormian bones ... "Al Gazali Sabrinathan Nair syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih. ... Articles with short description, Short description matches Wikidata, Genetic syndromes, Diseases named for discoverer). ... also known as Al Gazali-Nair syndrome is a very rare multi-systemic genetic disorder which is characterized by developmental ...

Those with injury or disease affecting the muscles, bones, ligaments, or tendons will benefit from assessment by a physical ... developmental, neuromuscular, skeletal, or acquired disorders/diseases. Treatments focus mainly on improving gross and fine ... These can include stroke, chronic back pain, Alzheimer's disease, Charcot-Marie-Tooth disease (CMT), ALS, brain injury, ... This includes providing treatment in circumstances where movement and function are threatened by aging, injury, disease, or ...