Continuation of pegvaliase treatment during pregnancy: A case report

Phenylalanine hydroxylase (PAH) deficiency is an inborn error of phenylalanine (Phe) metabolism that results in the buildup of dietary Phe to potentially toxic levels. Poorly controlled Phe levels in women of childbearing age are particularly worrisome due to the toxic effect of elevated Phe on feta...

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Detalles Bibliográficos
Autores principales: Boyer, Monica, Skaar, Janette, Sowa, Mary, Tureson, Justin R., Chapel-Crespo, Cristel C., Chang, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847948/
https://www.ncbi.nlm.nih.gov/pubmed/33552907
http://dx.doi.org/10.1016/j.ymgmr.2021.100713

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847948/
https://www.ncbi.nlm.nih.gov/pubmed/33552907
http://dx.doi.org/10.1016/j.ymgmr.2021.100713

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