Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screening

Background: In infancy multiple acyl-CoA dehydrogenase deficiency (MADD) is commonly a severe inherited metabolic disease caused by genetic defects in electron transfer flavoprotein (ETF) or ETF ubiquinone oxidoreductase. Both enzymes require flavin adenine dinucleotide (FAD) as a cofactor. Riboflav...

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Bibliografische gegevens

Hoofdauteurs:	Gwendolyn Gramer, Georg F. Hoffmann, Julia B. Hennermann
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	Elsevier 2021-06-01
Reeks:	Molecular Genetics and Metabolism Reports
Onderwerpen:	Newborn screening Multiple acyl-CoA dehydrogenase deficiency Vitamin B12 deficiency Maternal Mother and child health
Online toegang:	http://www.sciencedirect.com/science/article/pii/S221442692100032X
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