Telehealth and COVID-19: Empowering Standards of Management for Patients Affected by Phenylketonuria and Hyperphenylalaninemia

Phenylketonuria (PKU) and Hyperphenylalaninemia (HPA) are inborn errors of metabolism (IEM) due to mutations in the PAH gene resulting in increased blood phenylalanine (Phe) concentrations. Depending on the Phe levels, a lifelong dietary intervention may be needed. During the COVID-19 pandemic, find...

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Detalles Bibliográficos
Autores principales: Rovelli, Valentina, Zuvadelli, Juri, Paci, Sabrina, Ercoli, Vittoria, Re Dionigi, Alice, Selmi, Raed, Salvatici, Elisabetta, Cefalo, Graziella, Banderali, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622759/
https://www.ncbi.nlm.nih.gov/pubmed/34828453
http://dx.doi.org/10.3390/healthcare9111407

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622759/
https://www.ncbi.nlm.nih.gov/pubmed/34828453
http://dx.doi.org/10.3390/healthcare9111407

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