Iliac artery dissection and rupture in a patient with classic Ehlers-Danlos syndrome due to COL5A1 null variant.
J Vasc Surg Cases Innov Tech
; 10(3): 101443, 2024 Jun.
Article
em En
| MEDLINE
| ID: mdl-38572164
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.
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Base de dados:
MEDLINE
Idioma:
En
Revista:
J Vasc Surg Cases Innov Tech
Ano de publicação:
2024
Tipo de documento:
Article