Management and Outcomes of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD Deficiency): A Retrospective Chart Review

Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a rare genetic condition affecting the mitochondrial beta-oxidation of long-chain fatty acids. This study reports on the clinical outcomes of patients diagnosed by newborn screening with VLCAD deficiency comparing metabolic parameters, enz...

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Bibliografiska uppgifter
Huvudupphovsmän: Maria Al Bandari, Laura Nagy, Vivian Cruz, Stacy Hewson, Alomgir Hossain, Michal Inbar-Feigenberg
Materialtyp: Artikel
Språk:English
Publicerad: MDPI AG 2024-03-01
Serie:International Journal of Neonatal Screening
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Länkar:https://www.mdpi.com/2409-515X/10/2/29