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Management precautions for risk of obesity are necessary among infants with PKU carrying the rs113883650 variant of the LAT1 gene: A cross-sectional study

Patients with phenylketonuria (PKU), an inborn error of phenylalanine metabolism, require consistent treatment to avoid the brain toxicity caused by hyperphenylalaninemia. The treatment consists of life-long use of a low-phenylalanine diet, which aims at decreasing hyperphenylalaninemia and maintain...

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Detalles Bibliográficos
Autores principales: Bik-Multanowski, Miroslaw, Didycz, Bozena, Bik-Multanowska, Kinga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853486/
https://www.ncbi.nlm.nih.gov/pubmed/35176108
http://dx.doi.org/10.1371/journal.pone.0264084