Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Ehlers-Danlos syndrome, vascular type

MONDO:0017314

Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS.

Also known as: EDS IV, EDS type 4, Ehlers-Danlos syndrome type 4, Ehlers-Danlos syndrome type IV, Ehlers-Danlos syndrome, type IV, Ehlers-Danlos syndrome, vascular type, sack-Barabas syndrome, EDS IV (formerly)

6 clinical trials for this condition and its sub-types, 6 tagged with Ehlers-Danlos syndrome, vascular type itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by