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

Internet

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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