Treatment adherence during childhood in individuals with phenylketonuria: Early signs of treatment discontinuation

INTRODUCTION: Phenylketonuria (PKU) is an autosomal recessive disorder characterized by a deficiency in phenylalanine (Phe) hydroxylase activity. Early diagnosis and continuous treatment with a low Phe diet prevents severe neurological and cognitive impairment. AIMS: 1. Analyze how treatment adheren...

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Detalles Bibliográficos
Autores principales: García, María Ignacia, Araya, Gabriela, Coo, Soledad, Waisbren, Susan E., de la Parra, Alicia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412103/
https://www.ncbi.nlm.nih.gov/pubmed/28491816
http://dx.doi.org/10.1016/j.ymgmr.2017.04.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412103/
https://www.ncbi.nlm.nih.gov/pubmed/28491816
http://dx.doi.org/10.1016/j.ymgmr.2017.04.006

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