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Global prevalence of classic phenylketonuria based on Neonatal Screening Program Data: systematic review and meta-analysis

Phenylketonuria is a disease caused by congenital defects in phenylalanine metabolism that leads to irreversible nerve cell damage. However, its detection in the early days of life can reduce its severity. Thus, many countries have started disease screening programs for neonates. The present study a...

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Detalles Bibliográficos
Autores principales:	Shoraka, Hamid Reza, Haghdoost, Ali Akbar, Baneshi, Mohammad Reza, Bagherinezhad, Zohre, Zolala, Farzaneh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Pediatric Society 2020
Materias:	Systematic review and meta-analysis
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029670/ https://www.ncbi.nlm.nih.gov/pubmed/32024337 http://dx.doi.org/10.3345/kjp.2019.00465

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