CADASIL. Case report
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a hereditary cerebral arteriopathy caused by mutations in the Notch-3 gene. The diagnosis is reached by skin biopsy revealing presence of granular osmiophílic material (GOM), and/or by genetic tes...
Enregistré dans:
| Publié dans: | Dementia & Neuropsychologia |
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| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Associação Neurologia Cognitiva e do Comportamento
2012
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| Sujets: | |
| Accès en ligne: | https://www.redalyc.org/articulo.oa?id=339529038013 |
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