Nutrient Status among Latvian Children with Phenylketonuria

(1) Introduction: Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism. The main treatment for PKU is to manage nutrition, thereby restricting phenylalanine intake. Part of patient management is analyzing eating habits to substitute missing nutrients and limit the...

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Detalles Bibliográficos
Autores principales: Lubina, Olga, Gailite, Linda, Borodulina, Julija, Auzenbaha, Madara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297135/
https://www.ncbi.nlm.nih.gov/pubmed/37371168
http://dx.doi.org/10.3390/children10060936

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297135/
https://www.ncbi.nlm.nih.gov/pubmed/37371168
http://dx.doi.org/10.3390/children10060936

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