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Coexistence of Neurofibromatosis Type-1 and MTHFR C677T Gene Mutation in a Young Stroke Patient: A Case Report

In neurofibromatosis type-1 (NF1), cerebrovascular disorders are rarely encountered although vasculopathy is a well-known complication. Several mutations seen in methylenetetrahydrofolate reductase (MTHFR) give rise to the formation of hyperhomocysteinemia and homocystinuria, a considerable risk fac...

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Detalles Bibliográficos
Autores principales:	Yilmaz, Halim, Erkin, Gulten, Gumus, Haluk, Nalbant, Lutfiye
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600223/ https://www.ncbi.nlm.nih.gov/pubmed/23533858 http://dx.doi.org/10.1155/2013/735419

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