Persistent aura and status migrainosus in CADASIL syndrome: A case report

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary microangiopathy characterized by a genetic predisposition to small arteries of the brain. It is produced by a mutation in the NOTCH3 gene and concerns adults. The symptomatology is di...

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Detalles Bibliográficos
Autores principales: Hamid, Mohamed, Adraoui, Yassine El, Satte, Amal, Bourazza, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379942/
https://www.ncbi.nlm.nih.gov/pubmed/35982717
http://dx.doi.org/10.1016/j.radcr.2022.07.050

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379942/
https://www.ncbi.nlm.nih.gov/pubmed/35982717
http://dx.doi.org/10.1016/j.radcr.2022.07.050

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