Lipids and phenylketonuria: current evidences pointed the need for lipidomics studies

Phenylketonuria (PKU) is the most prevalent inborn error of amino acid metabolism. The disease is due to the deficiency of phenylalanine (Phe) hydroxylase activity, which causes the accumulation of Phe. Early diagnosis through neonatal screening is essential for early treatment implementation, avoid...

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Bibliographic Details
Main Author: Guerra, Inês M. S. (author)
Other Authors: Ferreira, Helena B. (author), Neves, Bruna (author), Melo, Tânia (author), Diogo, Luísa M. (author), Domingues, M. Rosário (author), Moreira, Ana S. P. (author)
Format: article
Language:eng
Published: 2021
Subjects:
Inborn errors of metabolism
Phenylketonuria
Lipid changes
Oxidative stress
Lipidomics
Mass spectrometry
Online Access:http://hdl.handle.net/10773/28697
Country:Portugal
Oai:oai:ria.ua.pt:10773/28697

Internet

http://hdl.handle.net/10773/28697

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