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Article

MR imaging findings of glutaric aciduria type II.

Singapore medical journal - 1 Apr 2010

Mumtaz H A, Gupta V, Singh P, Marwaha R K, Khandelwal N

Abstract excerpt

Glutaric aciduria type II, also known as multiple acyl coenzyme A dehydrogenase deficiency, is an autosomal recessive, mitochondrial organic acid disorder that impairs electron transfer flavoprotein (ETF) or ETF-ubiquinone oxidoreductase, and causes a defect in flavin metabolism or transport. It has a heterogeneous clinical presentation, with at least three different phenotypic appearances. Magnetic resonance...

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PMID: 20505899

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

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