Food Regime for Phenylketonuria: Presenting Complications and Possible Solutions

In the category of rare inherited genetic disorders, phenylketonuria is a prominent example. Here, the defective phenylalanine hydroxylase enzyme fails to catalyze conversion of phenylalanine to tyrosine. This leads to not only excess deposition of phenylalanine leading to phenylalanine toxicity but...

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Detalles Bibliográficos
Autores principales: Kumar Dalei, Sudipt, Adlakha, Nidhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785131/
https://www.ncbi.nlm.nih.gov/pubmed/35082498
http://dx.doi.org/10.2147/JMDH.S330845

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785131/
https://www.ncbi.nlm.nih.gov/pubmed/35082498
http://dx.doi.org/10.2147/JMDH.S330845

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