A Distinctive Metabolomics Profile and Potential Biomarkers for Very Long Acylcarnitine Dehydrogenase Deficiency (VLCADD) Diagnosis in Newborns

Very long-chain acylcarnitine dehydrogenase deficiency (VLCADD) is a rare inherited metabolic disorder associated with fatty acid <i>β</i>-oxidation and characterized by genetic mutations in the <i>ACADVL</i> gene and accumulations of acylcarnitines. VLCADD, developed in neon...

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Bibliographic Details
Main Authors:	Rajaa Sebaa, Reem H. AlMalki, Wafaa Alseraty, Anas M. Abdel Rahman
Format:	Article
Language:	English
Published:	MDPI AG 2023-06-01
Series:	Metabolites
Subjects:	VLCADD newborns untargeted metabolomics profiling potential biomarkers
Online Access:	https://www.mdpi.com/2218-1989/13/6/725

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