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
en 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.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Idioma:
En
Revista:
J Vasc Surg Cases Innov Tech
Año:
2024
Tipo del documento:
Article
Pais de publicación:
Estados Unidos