2020
DOI: 10.3892/mmr.2020.11524
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Clinical characteristics and gene mutation analysis of an adult patient with ETFDH‑related multiple acyl‑CoA dehydrogenase deficiency

Abstract: Multiple acyl-coa dehydrogenase deficiency (Madd) is a rare autosomal recessive disorder of fatty acid metabolism caused by defects in electron transfer flavoprotein (ETF) or electron transfer flavoprotein dehydrogenase (ETFDH). These defects are mainly classified into the neonatal and late-onset types, based on their clinical manifestations. ETFDH gene mutations are generally considered to be associated with the late-onset type. The present study reported an adult woman with late-onset Madd accompanied with b… Show more

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“…In these diseases, the administration of a high dose of CoQ10 is a common therapy even if a clear efficacy has not yet been proved. Moreover, a deficit in CoQ10 has been identified in some genetic disorders linked to lipid metabolism, such as Familial Hypercholesterolemia and MAAD (Multiple acyl-CoA Dehydrogenase Deficiency) [ 87 ]. In both these conditions, the administration of CoQ10 lead to a reduction in the atherosclerosis and to a reduction in muscle pain and fatigue.…”
Section: Ubiquinone/coenzyme Q Biosynthesismentioning
confidence: 99%
“…In these diseases, the administration of a high dose of CoQ10 is a common therapy even if a clear efficacy has not yet been proved. Moreover, a deficit in CoQ10 has been identified in some genetic disorders linked to lipid metabolism, such as Familial Hypercholesterolemia and MAAD (Multiple acyl-CoA Dehydrogenase Deficiency) [ 87 ]. In both these conditions, the administration of CoQ10 lead to a reduction in the atherosclerosis and to a reduction in muscle pain and fatigue.…”
Section: Ubiquinone/coenzyme Q Biosynthesismentioning
confidence: 99%