Ehlers-Danlos syndrome, dermatosparaxis type

A form of Ehlers-Danlos syndrome (EDS) characterized by extreme skin fragility and laxity, a prominent facial gestalt, excessive bruising and, sometimes, major complications due to visceral and vascular fragility.

Also known as: EDS VIIC, Ehlers-Danlos syndrome type 7C, Ehlers-Danlos syndrome, dermatosparaxis type, EDS 7C, EDS7C, EDSDERMS, Ehlers-Danlos syndrome type 7C (formerly), Ehlers-Danlos syndrome, type VII, autosomal recessive

0 clinical trials for this condition and its sub-types, 0 tagged with Ehlers-Danlos syndrome, dermatosparaxis type itself.