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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Bibliographic Details
Published in:Neurol Genet
Main Authors: Oluwole, Olusegun John, Ibrahim, Heba, Garozzo, Debora, Ben Hamouda, Karim, Ismail Mostafa Hassan, Saly, Hegazy, Ahmed Metwaly, Msaddi, Abdul Karim
Format: Artigo
Language:Inglês
Published: Wolters Kluwer 2019
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6936311/
https://ncbi.nlm.nih.gov/pubmed/32042911
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000382
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