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Article

Malonyl coenzyme A decarboxylase deficiency: early dietary restriction and time course of cardiomyopathy.

Pediatrics - 1 Aug 2012

Prada Carlos E, Jefferies John L, Grenier Michelle A, Huth Christina M, Page Kimberley I, Spicer Robert L, Towbin Jeffrey A, Leslie Nancy D

Abstract excerpt

Malonyl coenzyme A (CoA) decarboxylase (MCD) deficiency is a rare autosomal recessive organic acidemia characterized by varying degrees of organ involvement and severity. MCD regulates fatty acid biosynthesis and converts malonyl-CoA to acetyl-CoA. Cardiomyopathy is 1 of the leading causes of mor...

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Source

Identifiers

PMID: 22778304
DOI: 10.1542/peds.2011-2927

Genes

MLYCD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22778304-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Malonyl coenzyme A decarboxylase deficiency: early dietary restriction and time course of cardiomyopathy.PMID 22778304Read ↗

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