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Joint hypermobility syndrome
- Hypermobile joints often occur in otherwise healthy and normal children. This is called benign hypermobility syndrome. Rare medical conditions associated with hypermobile joints include: Cleidocranial dysostosis (abnormal development of bones in the skull ...
- ... syndrome.Some people with a condition called benign joint hypermobility syndrome (BJHS) also make a reduced amount of tenascin- ... joint pain. The signs and symptoms of benign joint hypermobility syndrome overlap significantly with those of the hypermobile type ...
- ... treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome. Am J Med Genet ...
- ... bent (camptodactyly) and an unusually large range of joint movement (hypermobility).People with Shprintzen-Goldberg syndrome often have delayed development and mild to moderate ...
- ... highly stretchy (elastic), and fragile; abnormal scarring; and joint hypermobility. Additionally, people with classical Ehlers-Danlos syndrome resulting from a COL1A1 gene mutation are prone ...
- Ehlers-Danlos Syndrome Hypermobility Type (Marfan Foundation) - PDFEhlers-Danlos Syndrome/Learn More ... Ehlers-Danlos Syndrome ... Marfan Foundation ... PDF
- Ehlers-Danlos Syndrome (National Library of Medicine)Ehlers-Danlos syndrome (EDS) is a group of inherited disorders that weaken connective tissues. Connective tissues are proteins that support skin, bones, blood ...
- ... abnormal scarring; and an unusually large range of joint movement (hypermobility). About 20 COL5A2 gene mutations have been identified in people with classical Ehlers-Danlos syndrome. These mutations, which affect one copy of the ...
- ... have an unusually large range of joint movement (hypermobility) or joint deformities (contractures) that restrict movement. People with Larsen syndrome can also have abnormal curvature of the spine ( ...
- ... abnormal scarring; and an unusually large range of joint movement (hypermobility). More than 100 COL5A1 gene mutations have been identified in people with classical Ehlers-Danlos syndrome. The mutations affect one copy of the gene ...
