New challenges in management of phenylketonuria in pregnancy: a case report

BACKGROUND: Phenylketonuria (PKU) is an autosomal recessive disease that belongs to a group of disorders resulting from inborn errors of protein metabolism. It was the first disease included in neonatal screening. Neonatal screening has allowed an early diagnosis and treatment of the disease. As a r...

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Detalles Bibliográficos
Autores principales: Ugalde-Abiega, Beatriz, Stanescu, Sinziana, Belanger, Amaya, Martinez-Pardo, Mercedes, Arrieta, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10633903/
https://www.ncbi.nlm.nih.gov/pubmed/37941064
http://dx.doi.org/10.1186/s13256-023-04209-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10633903/
https://www.ncbi.nlm.nih.gov/pubmed/37941064
http://dx.doi.org/10.1186/s13256-023-04209-0

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