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...

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Detalles Bibliográficos
Autores principales: da Silva, Julio Cesar Vasconcelos, Gasparetto, Emerson L., Engelhardt, Eliasz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Neurologia Cognitiva e do Comportamento 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618968/
https://www.ncbi.nlm.nih.gov/pubmed/29213795
http://dx.doi.org/10.1590/S1980-57642012DN06030013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618968/
https://www.ncbi.nlm.nih.gov/pubmed/29213795
http://dx.doi.org/10.1590/S1980-57642012DN06030013

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