Recurrent generalized seizures as the prominent manifestation in a patient with CADASIL: a case report and literature review

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited arteriopathy typically caused by mutations in the NOTCH-3 gene. Few detailed descriptions of recurrent generalized seizures in CADASIL has been reported. CASE PRESENTATION...

Descripción completa

Detalles Bibliográficos
Autores principales: Pan, Liuhua, Chen, Yan, Zhao, Shanshan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526332/
https://www.ncbi.nlm.nih.gov/pubmed/36180846
http://dx.doi.org/10.1186/s12883-022-02889-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526332/
https://www.ncbi.nlm.nih.gov/pubmed/36180846
http://dx.doi.org/10.1186/s12883-022-02889-7

Ejemplares similares