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Vascular type Ehlers-Danlos Syndrome with fatal spontaneous rupture of a right common iliac artery dissection: case report and review of literature

Vascular Ehlers-Danlos Syndrome (previously Ehlers-Danlos IV) is a rare autosomal dominant collagen vascular disorder caused by a 2q31 COL3A1 gene mutation encoding pro-alpha1 chain of type III collagen (in contrast to classic Ehlers-Danlos, caused by a COL5A1 mutation). The vascular type accounts f...

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Autores principales: Abayazeed, Aly, Hayman, Emily, Moghadamfalahi, Mana, Cain, Darren
Formato: Artigo
Lenguaje:Inglês
Publicado: EduRad 2014
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4037255/
https://ncbi.nlm.nih.gov/pubmed/24967021
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3941/jrcr.v8i2.1568
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