Behavioral and Emotional Problems in Early-Treated Brazilian Children and Adolescents with Phenylketonuria

BACKGROUND: Phenylketonuria (PKU) is an inborn error of metabolism caused by mutations in the phenylalanine hydroxylase (PAH) gene. When untreated, PKU leads to a significant intellectual deficiency. Although early initiation of dietary therapy allows normal cognitive development, low adherence to t...

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Detalles Bibliográficos
Autores principales: Neto, Eduardo Vieira, de Souza Maia Filho, Heber, Monteiro, Claudia Braga, de Mattos Carvalho, Lilian, da Cruz, Thuane Silva, de Barros, Belisia Vasconcelos, Ribeiro, Márcia Gonçalves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2018
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354646/
https://www.ncbi.nlm.nih.gov/pubmed/30375370
http://dx.doi.org/10.12659/MSM.909146

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354646/
https://www.ncbi.nlm.nih.gov/pubmed/30375370
http://dx.doi.org/10.12659/MSM.909146

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