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

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...

Full description

Bibliographic Details
Main Authors: Mohamed Hamid, (MD), Yassine El Adraoui, (MD), Amal Satte, (MD), Ahmed Bourazza, (MD)
Format: Article
Language:English
Published: Elsevier 2022-10-01
Series:Radiology Case Reports
Subjects:
CADASIL
Aura
Status migrainosus
Genetic test
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043322005957

Similar Items

Similar Items