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Cadasil - genetic and ultrastructural diagnosis. Case report
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a hereditary disorder which affects the cerebral vasculature due to mutations in the NOTCH 3 gene. The diagnosis may be established through genetic testing for detection of these mutations and/or...
Autores principales: | da Silva, Julio Cesar Vasconcelos, Chimelli, Leila, Sudo, Felipe Kenji, Engelhardt, Eliasz |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação de Neurologia Cognitiva e do
Comportamento
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619327/ https://www.ncbi.nlm.nih.gov/pubmed/29213994 http://dx.doi.org/10.1590/1980-57642015DN94000428 |
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