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Hypermobility spectrum disorder does not include people with asymptomatic hypermobility or people with double-jointedness but no other symptoms. Hypermobile Ehlers–Danlos syndrome and hypermobility spectrum disorders may be equally severe. [5] [6] HSD is further classified into different subtypes, which include: [6]
Joint hypermobility syndrome shares symptoms with other conditions such as Marfan syndrome, Ehlers-Danlos Syndrome, and osteogenesis imperfecta. Experts in connective tissue disorders formally agreed that severe forms of Hypermobility Syndrome and mild forms of Ehlers-Danlos Syndrome Hypermobility Type are the same disorder. [citation needed]
Marfan syndrome, cutis laxa syndrome, familial joint hypermobility syndrome, [4] Loeys–Dietz syndrome, hypermobility spectrum disorder: Treatment: Supportive [6] Prognosis: Depends on specific disorder [4] Frequency: 1 in 5,000 [1]
Babinski–Nageotte syndrome; Baboon syndrome; Baggio–Yoshinari syndrome; Baller–Gerold syndrome; Bamforth–Lazarus syndrome; Bangstad syndrome; Bannayan–Riley–Ruvalcaba syndrome
Hypermobility may refer to: Hypermobility (joints) , joints that stretch further than normal Hypermobility spectrum disorder , a heritable connective tissue disorder
This is a group of diseases and disorders that involve the fascia. ... This list may not reflect recent changes. A. ... Hypermobility (joints) I. Ischemic fasciitis; L.
Neuromuscular disease can be caused by autoimmune disorders, [1] genetic/hereditary disorders [2] and some forms of the collagen disorder Ehlers–Danlos syndrome, [12] exposure to environmental chemicals and poisoning which includes heavy metal poisoning. [3]
May either present as an isolated trait, or be a symptom of a condition such as a hypermobility spectrum disorder [medical citation needed] Risk factors: Family history: Frequency: 24–36% of the U.S. population [3]