A Patient with Combined CADASIL and MTHFR Homozygosity

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is an inherited disorder caused by a mutation in the NOTCH 3 gene, characterized by early onset of subcortical lacunar infarcts in the absence of vascular risk factors and cerebral microbleeds. Homoz...

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Detalles Bibliográficos
Autores principales: Ibrikji, Sidonie, El Halabi, Tarek, Yamout, Bassem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048904/
https://www.ncbi.nlm.nih.gov/pubmed/32128266
http://dx.doi.org/10.1155/2020/4980847

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048904/
https://www.ncbi.nlm.nih.gov/pubmed/32128266
http://dx.doi.org/10.1155/2020/4980847

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