A case of recurrent intracranial hemorrhage in CADASIL caused by NOTCH3 c.1759C>T heterozygous mutation

BACKGROUND: Cerebral autosomal‐dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a cerebrovascular disease that is closely related to the NOTCH3 gene. Recurrent ischemic stroke, progressive cognitive dysfunction, and mental symptoms are the main clinical manifestat...

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Detalles Bibliográficos
Autores principales: Chu, Ying, Wang, Qi, Ma, Yue, Xu, Linying, Ren, Kexin, Liu, Jiahui, Tao, Dingbo, Cao, Hua, Ji, Xiaofei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937875/
https://www.ncbi.nlm.nih.gov/pubmed/36604800
http://dx.doi.org/10.1002/jcla.24840

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937875/
https://www.ncbi.nlm.nih.gov/pubmed/36604800
http://dx.doi.org/10.1002/jcla.24840

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