Hydrocephalus presented as the prominent symptom of severe 5,10-methylenetetrahydrofolate reductase deficiency in an infant: A case report

Hyperhomocysteinemia is a common medical condition observed in patients with aminoaciduria. Deficiency in cystathionine beta-synthase, metabolism of cobalamin associated C, peroxiredoxin 1, 5-methyltetrahydrofolate-homocysteine methyltransferase reductase, LMBR1 domain containing 1, 5-methyltetrahyd...

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Detalles Bibliográficos
Autores principales: Ding, Yuan, Wang, Qiao, Gong, Chun-Xiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829199/
https://www.ncbi.nlm.nih.gov/pubmed/36699103
http://dx.doi.org/10.3892/mi.2022.37

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829199/
https://www.ncbi.nlm.nih.gov/pubmed/36699103
http://dx.doi.org/10.3892/mi.2022.37

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