Article
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.
Annals of the New York Academy of Sciences - 26 Sept 1997
Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Maréchal E, Maciazek J, Vayssière C, Cruaud C, Cabanis E A, Ruchoux M M, Weissenbach J, Bach J F, Bousser M G, Tournier-Lasserve E
Abstract excerpt
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited condition whose key features include recurrent subcortical ischemic events, migraine attacks and vascular dementia in association with diffuse white-matter abnormalities seen on ne...
Topics
- Adult
- Cerebral Arterial Diseases
- Cerebral Infarction
- Chromosomes, Human, Pair 19
- Dementia, Vascular
- Genes, Dominant
- Genetic Linkage
- Humans
- Leukoencephalopathy, Progressive Multifocal