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Multiple Acyl Coenzyme A Dehydrogenase Deficiency Summary

Description: An autosomal recessive disorder of fatty acid oxidation, and branched chain amino acids (AMINO ACIDS, BRANCHED-CHAIN); LYSINE; and CHOLINE catabolism, that is due to defects in either subunit of ELECTRON TRANSFER FLAVOPROTEIN or its dehydrogenase, electron transfer flavoprotein-ubiquinone oxidoreductase (EC 1.5.5.1).

Also Known As: ETFA Deficiency; ETFB Deficiency; ETFDH Deficiency; Electron Transfer Flavoprotein Alpha Subunit Deficiency; Electron Transfer Flavoprotein Beta Subunit Deficiency Show All >>

Networked: 165 relevant articles (5 outcomes, 11 trials/studies) for this Disease

Key Drugs and Agents for Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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Drugs and Important Biological Agents (IBA) related to treatments:

Riboflavin (Vitamin B2) : 3 outcomes 2 studies in 42 results : FDA 8 Generic
Carnitine (L-Carnitine) : 2 outcomes 3 studies in 27 results : FDA 9 Generic
Glycine (Aminoacetic Acid) : 2 outcomes in 2 results : FDA 23 Generic
Acids : 1 outcome 2 studies in 12 results : IBA
Enzymes : 1 outcome in 5 results : IBA
Mitochondrial Proteins (Mitochondrial Protein) : 1 outcome in 1 result : IBA
Acyl Coenzyme A (Acyl CoA) : 2 studies in 18 results : IBA
Electron-Transferring Flavoproteins (Electron Transfer Flavoprotein) : 1 study in 24 results : IBA
Oxidoreductases : 1 study in 22 results : IBA
Medium chain acyl CoA dehydrogenase deficiency : 1 study in 13 results : IBA

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Diseases Related to Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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Key Therapies for Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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