CARASIL
HTRA1
carriers
heritability
vascular dementia
Journal
Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899
Informations de publication
Date de publication:
2020
2020
Historique:
received:
08
02
2020
accepted:
14
05
2020
entrez:
29
7
2020
pubmed:
29
7
2020
medline:
29
7
2020
Statut:
epublish
Résumé
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is clinically characterized by early-onset dementia, stroke, spondylosis deformans, and alopecia. In CARASIL cases, brain magnetic resonance imaging reveals severe white matter hyperintensities (WMHs), lacunar infarctions, and microbleeds. CARASIL is caused by a homozygous mutation in
Identifiants
pubmed: 32719647
doi: 10.3389/fneur.2020.00545
pmc: PMC7351529
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
545Informations de copyright
Copyright © 2020 Uemura, Nozaki, Kato, Koyama, Sakai, Ando, Kanazawa, Hishikawa, Nishimoto, Polavarapu, Nalini, Hanazono, Kuzume, Shindo, El-Ghanem, Abe, Sato, Yoshida, Ikeuchi, Mizuta, Mizuno and Onodera.
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