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A form of Ehlers-Danlos syndrome, a connective tissue disorder characterized by hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity. EDSARTH1 is an autosomal dominant form characterized by frequent congenital hip dislocation and extreme joint laxity with recurrent joint subluxations and minimal skin involvement.




Arthrochalasis multiplex congenita
EDS VII mutant procollagen type
Ehlers-Danlos syndrome 7A
Ehlers-Danlos syndrome arthrochalasic type
Ehlers-Danlos syndrome type VIIA, autosomal dominant


Ehlers-Danlos syndrome


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