Ehlers-Danlos syndrome, arthrochalasic type

Ehlers-Danlos syndrome, arthrochalasic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of Hereditary connective tissue Diseases characterized by Joint hyperlaxity, cutaneous hyperelasticity and Tissue fragility, and is marked by bilateral congenital hip dislocation, hyperlaxity of the joints, and Recurrent partial dislocations. Other signs include hyperextensible skin, Fragile tissues with atrophic scars, and Muscular hypotonia.

Also Known As

  • Ehlers-Danlos syndrome type 7
  • 14951 0.630708932877