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Results 1 - 10 of 18 for Joint hypermobility
  1. TNXB gene 
    ... syndrome.Some people with a condition called benign joint hypermobility syndrome (BJHS) also make a reduced amount of ... joint pain. The signs and symptoms of benign joint hypermobility syndrome overlap significantly with those of the hypermobile ...
    https://medlineplus.gov/genetics/gene/tnxb - Genetics
  2. Anauxetic dysplasia 
    ... other skeletal abnormalities, an unusually large range of joint movement (hypermobility), dental problems, and distinctive facial features. Mild intellectual ...
    https://medlineplus.gov/genetics/condition/anauxetic-dysplasia - Genetics
  3. Ehlers-Danlos syndrome 
    ... treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome. Am J Med ...
    https://medlineplus.gov/genetics/condition/ehlers-danlos-syndrome -
  4. COL1A1 gene 
    ... highly stretchy (elastic), and fragile; abnormal scarring; and joint hypermobility. Additionally, people with classical Ehlers-Danlos syndrome resulting ...
    https://medlineplus.gov/genetics/gene/col1a1 - Genetics
  5. COL1A2 gene 
    ... in the heart, highly stretchy (elastic) skin, and joint hypermobility. The mutations that cause this form of the ...
    https://medlineplus.gov/genetics/gene/col1a2 - Genetics
  6. Familial thoracic aortic aneurysm and dissection 
    ... skin, an unusually large range of joint movement (joint hypermobility), and either a sunken or protruding chest. Occasionally, ...
    https://medlineplus.gov/...l-thoracic-aortic-aneurysm-and-dissection - Genetics
  7. Larsen syndrome 
    ... condition may have an unusually large range of joint movement (hypermobility) or joint deformities (contractures) that restrict movement. People with Larsen ...
    https://medlineplus.gov/genetics/condition/larsen-syndrome - Genetics
  8. Trichorhinophalangeal syndrome type II 
    ... II often have an unusually large range of joint movement (hypermobility). However, as osteochondromas begin to develop, typically starting between infancy and mid-childhood, the joints begin to stiffen, leading to decreased mobility. Individuals ...
    https://medlineplus.gov/.../trichorhinophalangeal-syndrome-type-ii - Genetics
  9. Spondylocarpotarsal synostosis syndrome 
    ... flat feet, or an unusually large range of joint movement (hypermobility). Individuals with this disorder can survive into adulthood. Intelligence is generally unaffected, although mild developmental delay has been reported ... disrupt vertebral segmentation, joint formation and skeletogenesis. Nat Genet. 2004 Apr;36( ...
    https://medlineplus.gov/.../spondylocarpotarsal-synostosis-syndrome - Genetics
  10. Hajdu-Cheney syndrome 
    ... joint abnormalities, particularly an unusually large range of joint movement (hypermobility); dental problems; hearing loss; a deep, gravelly voice; ...
    https://medlineplus.gov/genetics/condition/hajdu-cheney-syndrome - Genetics
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