Cerebral small vessel disease due to a unique heterozygous HTRA1 mutation in an African man

OBJECTIVE: To describe the case of an African patient who was diagnosed with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL). METHODS: Case report and literature review. RESULTS: We present a 39-year-old Gabonese man who developed progressive gai...

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Detalles Bibliográficos
Autores principales: Oluwole, Olusegun John, Ibrahim, Heba, Garozzo, Debora, Ben Hamouda, Karim, Ismail Mostafa Hassan, Saly, Hegazy, Ahmed Metwaly, Msaddi, Abdul Karim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936311/
https://www.ncbi.nlm.nih.gov/pubmed/32042911
http://dx.doi.org/10.1212/NXG.0000000000000382

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936311/
https://www.ncbi.nlm.nih.gov/pubmed/32042911
http://dx.doi.org/10.1212/NXG.0000000000000382

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