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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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
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author Hamid, Mohamed
Adraoui, Yassine El
Satte, Amal
Bourazza, Ahmed
author_facet Hamid, Mohamed
Adraoui, Yassine El
Satte, Amal
Bourazza, Ahmed
author_sort Hamid, Mohamed
collection PubMed
description 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 diversified including migraines with or without aura, subcortical ischemic events, and cognitive impairment. The diagnosis of CADASIL is suspected by neuroimaging and confirmed by genetic testing. Treatment of the disease remains preventive. We report a case of CADASIL manifesting as status migrainosus with persistent aura.
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spelling pubmed-93799422022-08-17 Persistent aura and status migrainosus in CADASIL syndrome: A case report Hamid, Mohamed Adraoui, Yassine El Satte, Amal Bourazza, Ahmed Radiol Case Rep 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 diversified including migraines with or without aura, subcortical ischemic events, and cognitive impairment. The diagnosis of CADASIL is suspected by neuroimaging and confirmed by genetic testing. Treatment of the disease remains preventive. We report a case of CADASIL manifesting as status migrainosus with persistent aura. Elsevier 2022-08-10 /pmc/articles/PMC9379942/ /pubmed/35982717 http://dx.doi.org/10.1016/j.radcr.2022.07.050 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Hamid, Mohamed
Adraoui, Yassine El
Satte, Amal
Bourazza, Ahmed
Persistent aura and status migrainosus in CADASIL syndrome: A case report
title Persistent aura and status migrainosus in CADASIL syndrome: A case report
title_full Persistent aura and status migrainosus in CADASIL syndrome: A case report
title_fullStr Persistent aura and status migrainosus in CADASIL syndrome: A case report
title_full_unstemmed Persistent aura and status migrainosus in CADASIL syndrome: A case report
title_short Persistent aura and status migrainosus in CADASIL syndrome: A case report
title_sort persistent aura and status migrainosus in cadasil syndrome: a case report
topic Case Report
url 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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