Arthrochalasia Ehlers-Danlos syndrome

What is Arthrochalasia Ehlers-Danlos syndrome?

A form of Ehlers-Danlos syndrome (EDS) characterized by congenital bilateral hip dislocation, severe generalized joint hypermobility with recurrent joint dislocations and subluxations, hyperextensible and/or fragile skin.

Other condition names

  • Arthrochalasis multiplex congenita
  • Ehlers-Danlos syndrome type 7
  • Ehlers-Danlos syndrome, arthrochalasia type
  • aEDS

Inheritance type

Autosomal dominant


  • Worldwide: Unknown

Age of Onset

  • Infancy
  • Neonatal
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