Multiple Acyl Coenzyme A Dehydrogenase Deficiency
"Multiple Acyl Coenzyme A Dehydrogenase Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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).
MeSH Number(s)
C16.320.565.100.614
C18.452.648.100.614
C18.452.660.612
Concept/Terms
Multiple Acyl Coenzyme A Dehydrogenase Deficiency- Multiple Acyl Coenzyme A Dehydrogenase Deficiency
- MADD (Multiple Acyl-CoA Dehydrogenase Deficiency)
- MADD (Multiple Acyl CoA Dehydrogenase Deficiency)
- MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency)
- Glutaric Aciduria II
- Ethylmalonic-Adipic Aciduria
- Aciduria, Ethylmalonic-Adipic
- Acidurias, Ethylmalonic-Adipic
- Ethylmalonic Adipic Aciduria
- Ethylmalonic-Adipic Acidurias
- Electron Transfer Flavoprotein Deficiency
- Glutaric Aciduria Type 2
- Glutaric Aciduria Type II
- Multiple Acyl-CoA Dehydrogenase Deficiency
- Multiple Acyl CoA Dehydrogenase Deficiency
- Ethylmalonic-Adipicaciduria
- Ethylmalonic Adipicaciduria
Glutaric Aciduria IIB- Glutaric Aciduria IIB
- ETFB Deficiency
- ETFB Deficiencies
- Electron Transfer Flavoprotein Beta Subunit Deficiency
Glutaric Aciduria IIC- Glutaric Aciduria IIC
- ETFDH Deficiency
- ETFDH Deficiencies
- Electron Transfer Flavoprotein Dehydrogenase Deficiency
Glutaric Aciduria IIA- Glutaric Aciduria IIA
- ETFA Deficiency
- ETFA Deficiencies
- Electron Transfer Flavoprotein Alpha Subunit Deficiency
Below are MeSH descriptors whose meaning is more general than "Multiple Acyl Coenzyme A Dehydrogenase Deficiency".
Below are MeSH descriptors whose meaning is more specific than "Multiple Acyl Coenzyme A Dehydrogenase Deficiency".
This graph shows the total number of publications written about "Multiple Acyl Coenzyme A Dehydrogenase Deficiency" by people in Harvard Catalyst Profiles by year, and whether "Multiple Acyl Coenzyme A Dehydrogenase Deficiency" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2009 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
2019 | 1 | 0 | 1 |
Below are the most recent publications written about "Multiple Acyl Coenzyme A Dehydrogenase Deficiency" by people in Profiles.
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Proximal muscle weakness. Pract Neurol. 2019 Aug; 19(4):321-325.
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Encephalopathy associated with a reversible splenial lesion in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. Rev Neurol (Paris). 2018 Dec; 174(10):747-750.
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A Term Newborn with Respiratory Distress, Acidosis, and Hypoglycemia. Clin Chem. 2017 02; 63(2):613-615.
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Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency. Am J Hum Genet. 2016 Jun 02; 98(6):1130-1145.
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Multi-organ abnormalities and mTORC1 activation in zebrafish model of multiple acyl-CoA dehydrogenase deficiency. PLoS Genet. 2013 Jun; 9(6):e1003563.
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Update on clinical aspects and treatment of selected vitamin-responsive disorders II (riboflavin and CoQ 10). J Inherit Metab Dis. 2012 Jul; 35(4):679-87.
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A case of late onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting as recurrent rhabdomyolysis and acute renal failure. Intern Med. 2011; 50(21):2663-8.
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Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD). PLoS One. 2009 Dec 17; 4(12):e8329.
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Evidence for a synergistic action of glutaric and 3-hydroxyglutaric acids disturbing rat brain energy metabolism. Int J Dev Neurosci. 2007 Oct; 25(6):391-8.