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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Detalles Bibliográficos
Autores principales: Lahkim, Mohamed, Laamrani, Fatima Zahare, Andour, Hajar, Gharbaoui, Yasmine, Sanhaji, Latifa, El-Fenni, Jamal, En-Nouali, Hassane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450197/
https://www.ncbi.nlm.nih.gov/pubmed/34584593
http://dx.doi.org/10.1016/j.radcr.2021.08.023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450197/
https://www.ncbi.nlm.nih.gov/pubmed/34584593
http://dx.doi.org/10.1016/j.radcr.2021.08.023

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