Phenylketonuria: central nervous system and microbiome interaction

Phenylketonuria (PKU) is an autosomal recessive inborn error of metabolism characterized by increased phenylalanine (Phe) levels causing an inadequate neurodevelopment; the treatment of PKU is a Phe-restricting diet, and as such it can modulate the intestinal microbiome of the individual, generating...

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Bibliographic Details
Main Author: Demian Arturo Herrera Morban
Format: Article
Language:English
Published: Hygeia Press di Corridori Marinella 2017-06-01
Series:Journal of Pediatric and Neonatal Individualized Medicine
Subjects:
Online Access:https://www.jpnim.com/index.php/jpnim/article/view/475