Long-term dietary intervention with low Phe and/or a specific nutrient combination improve certain aspects of brain functioning in phenylketonuria (PKU)

INTRODUCTION: In phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes accumulation of phenylalanine (Phe) in blood and brain. Although early introduction of a Phe-restricted diet can prevent severe symptoms from developing, patients who are diagnosed and treated early...

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Detalles Bibliográficos
Autores principales: Bruinenberg, Vibeke M., van Vliet, Danique, van der Goot, Els, Counotte, Danielle S., Kuhn, Mirjam, van Spronsen, Francjan J., van der Zee, Eddy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420157/
https://www.ncbi.nlm.nih.gov/pubmed/30875376
http://dx.doi.org/10.1371/journal.pone.0213391

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420157/
https://www.ncbi.nlm.nih.gov/pubmed/30875376
http://dx.doi.org/10.1371/journal.pone.0213391

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