Cadasil syndrome: A case report with a literature review

“CADASIL” is a genetic microangiopathy with autosomal dominant inheritance. Its epidemiology and physiopathogenesis are poorly specified, but it is proven that this disease is due to a mutation of the NOTCH3 gene resulting in a loss of elasticity of the media of the affected vessels. The clinical ex...

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Bibliographic Details
Main Authors: Mohamed Lahkim, PHC - Val de Grâce, Assistant Professor, PHD Std, Fatima Zahare Laamrani, Hajar Andour, Yasmine Gharbaoui, Latifa Sanhaji, Jamal El-Fenni, Hassane En-Nouali
Format: Article
Language:English
Published: Elsevier 2021-11-01
Series:Radiology Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043321005926