Hyperhomocysteinemia in men with a reproductive history of fetal neural tube defects: Three case reports and literature review

RATIONALE: Hereditary hyperhomocysteinemia results from a polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene that reduces folate metabolism. Mutations in the MTHFR gene are common in parents who have given birth to children with neural tube defects (NTDs). Most research has focused...

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Detalles Bibliográficos
Autores principales: Yu, Yang, Jia, Chunshu, Shi, Qingyang, Zhu, Yueying, Liu, Yanhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336619/
https://www.ncbi.nlm.nih.gov/pubmed/30633186
http://dx.doi.org/10.1097/MD.0000000000013998

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336619/
https://www.ncbi.nlm.nih.gov/pubmed/30633186
http://dx.doi.org/10.1097/MD.0000000000013998

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