Burden of phenylketonuria in Latin American patients: a systematic review and meta-analysis of observational studies

BACKGROUND: Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency of the enzyme phenylalanine hydroxylase. If untreated, the complications of PKU lead to significant neucognitive and neuropsychiatric impairments, placing a burden on both the individual’s quality of life and o...

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Detalles Bibliográficos
Autores principales: Pessoa, A. L. S., Martins, A. M., Ribeiro, E. M., Specola, N., Chiesa, A., Vilela, D., Jurecki, E., Mesojedovas, D., Schwartz, I. V. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338521/
https://www.ncbi.nlm.nih.gov/pubmed/35907851
http://dx.doi.org/10.1186/s13023-022-02450-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338521/
https://www.ncbi.nlm.nih.gov/pubmed/35907851
http://dx.doi.org/10.1186/s13023-022-02450-2

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