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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Korean Pediatric Society
2020
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| Materias: | |
| 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 |