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...
Huvudupphovsmän: | , , , , , |
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Materialtyp: | Artikel |
Språk: | English |
Publicerad: |
MDPI AG
2024-03-01
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Serie: | International Journal of Neonatal Screening |
Ämnen: | |
Länkar: | https://www.mdpi.com/2409-515X/10/2/29 |