Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report

Title
Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report
Authors
Keywords
Flavin adenine dinucleotide synthase deficiency, Multiple acyl-CoA dehydrogenase deficiency, Glutaric acidemia type II, FLAD1, Riboflavin, Newborn screening, Infantile onset, Lactic acidosis, Mitochondrial disease, Bulbar palsy
Journal
BRAIN & DEVELOPMENT
Volume -, Issue -, Pages -
Publisher
Elsevier BV
Online
2019-04-12
DOI
10.1016/j.braindev.2019.04.002

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