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 <i>PAH</i> gene resulting in increased blood phenylalanine (Phe) concentrations. Depending on the Phe levels, a lifelong dietary intervention may be needed. During the COVI...

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Autores principales: Valentina Rovelli, Juri Zuvadelli, Sabrina Paci, Vittoria Ercoli, Alice Re Dionigi, Raed Selmi, Elisabetta Salvatici, Graziella Cefalo, Giuseppe Banderali
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
PKU
HPA
R
Acceso en línea:https://doaj.org/article/f58748ea40f0415aab514bad15139e0c
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