%0 Case Reports
%T Iliac artery dissection and rupture in a patient with classic Ehlers-Danlos syndrome due to COL5A1 null variant.
%A Pujari A
%A Shalhub S
%J J Vasc Surg Cases Innov Tech
%V 10
%N 3
%D 2024 Jun
%M 38572164
暂无%R 10.1016/j.jvscit.2024.101443
%X This is a case of a 46-year-old woman who presented with right common iliac artery dissection preceded by a left common iliac artery dissection and rupture 6 years earlier. Both iliac arteries required repair. Based on her presentation, she met the clinical diagnostic criteria for vascular Ehlers-Danlos syndrome; however, the genetic workup demonstrated that she had classic Ehlers-Danlos syndrome due to a null variant in COL5A1, which is rarely associated with arteriopathy.