{Reference Type}: Case Reports
{Title}: Iliac artery dissection and rupture in a patient with classic Ehlers-Danlos syndrome due to COL5A1 null variant.
{Author}: Pujari A;Shalhub S;
{Journal}: J Vasc Surg Cases Innov Tech
{Volume}: 10
{Issue}: 3
{Year}: 2024 Jun
暂无{DOI}: 10.1016/j.jvscit.2024.101443
{Abstract}: 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.