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Multiple Acyl Coenzyme A Dehydrogenase Deficiency

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; Electron Transfer Flavoprotein Deficiency; Electron Transfer Flavoprotein Dehydrogenase Deficiency; Ethylmalonic-Adipic Aciduria; Ethylmalonic-Adipicaciduria; Glutaric Acidemia Type II; Glutaric Acidemia, Type 2; Glutaric Aciduria II; Glutaric Aciduria IIA; Glutaric Aciduria IIB; Glutaric Aciduria IIC; Glutaric Aciduria Type 2; Glutaric Aciduria Type II; Glutaric Aciduria, Type 2; MADD (Multiple Acyl-CoA Dehydrogenase Deficiency); Multiple Acyl-CoA Dehydrogenase Deficiency; Multiple FAD Dehydrogenase Deficiency; Aciduria, Ethylmalonic-Adipic; Acidurias, Ethylmalonic-Adipic; ETFA Deficiencies; ETFB Deficiencies; ETFDH Deficiencies; Ethylmalonic Adipic Aciduria; Ethylmalonic Adipicaciduria; Ethylmalonic-Adipic Acidurias; MADD (Multiple Acyl CoA Dehydrogenase Deficiency); MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency); Multiple Acyl CoA Dehydrogenase Deficiency
Networked: 323 relevant articles (11 outcomes, 15 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Muscle Weakness
2. Glycogen Storage Disease Type V (McArdle's Disease)
3. Delayed Hypersensitivity (Hypersensitivity, Type IV)
4. Medium chain acyl CoA dehydrogenase deficiency
5. Methylmalonic acidemia

Experts

1. Angelini, Corrado: 9 articles (01/2021 - 03/2006)
2. Yamaguchi, Seiji: 7 articles (08/2019 - 10/2002)
3. Liang, Wen-Chen: 5 articles (02/2021 - 09/2004)
4. Missaglia, Sara: 5 articles (01/2021 - 01/2018)
5. Tavian, Daniela: 5 articles (01/2021 - 01/2018)
6. Wanders, Ronald J A: 5 articles (01/2021 - 12/2005)
7. Hasegawa, Yuki: 5 articles (08/2019 - 10/2002)
8. Dorland, L: 5 articles (10/2010 - 10/2002)
9. Barile, Maria: 4 articles (07/2022 - 03/2006)
10. Fukuda, Seiji: 4 articles (08/2019 - 05/2008)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Multiple Acyl Coenzyme A Dehydrogenase Deficiency:
1. Riboflavin (Vitamin B2)FDA LinkGeneric
2. Carnitine (L-Carnitine)FDA LinkGeneric
3. Systemic carnitine deficiencyIBA
4. Glycine (Aminoacetic Acid)FDA LinkGeneric
5. AcidsIBA
6. EnzymesIBA
7. 4,6-dinitro-o-cresol (DNOC)IBA
8. acylcarnitineIBA
9. ethylmalonic acid (ethylmalonate)IBA
10. glutaric acidIBA

Therapies and Procedures

1. Aftercare (After-Treatment)
2. Therapeutics
3. Critical Care (Surgical Intensive Care)
4. Protein-Restricted Diet (Diet, Protein Restricted)
5. Fat-Restricted Diet (Diet, Fat Restricted)