Eds vascular type

Since then, other names have been used to describe it: Familial Acrogeria, Sack-Barabas Syndrome, Ehlers-Danlos Syndrome, type IV andor vascular type. Vascular EDS is particularly serious because of the risk for spontaneous arterial or organ rupture. Vascular Ehlers-Danlos syndrome is typically caused by a change (mutation) in the COL3Agene.

Rarely, it may be caused by a mutation in the COL1Agene. Vascular Ehlers-Danlos Syndrome (vEDS) A German physician named Georg Sack first recognized it in 19and named it Status Dysvascularis. Vascular Ehlers-Danlos Syndrome (vEDS) is characterized by thin, translucent skin easy bruising characteristic facial appearance (in some individuals and arterial, intestinal, andor uterine fragility.

The Ehlers-Danlos Syndrome

Vascular dissection or rupture, gastrointestinal perforation, or organ rupture are the presenting signs in the majority of adults identified to have vEDS. The Ehlers-Danlos Syndrome All of the Ehlers-Danlos Syndrome types share these characteristics, but each form has additional symptoms (for instance, the rupture of arteries common in vascular EDS). They are generally characterized by joint hypermobility (joints that stretch further than normal skin hyperextensibility (skin that can be stretched further than normal and tissue fragility). The COL3Agene provides instructions for making a component of type III collagen.

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