Literature DB >> 33745485

Malonyl coenzyme A decarboxylase deficiency with a novel mutation.

Cigdem S Kasapkara1, Burcu Civelek Ürey2, Ahmet C Ceylan3, Özlem Ünal Uzun2, Ibrahim İ Çetin4.   

Abstract

Malonyl-CoA, a product of acetyl-CoA carboxylase is a metabolic intermediate in lipogenic tissues that include liver and adipose tissue, where it is involved in the de novo fatty acid synthesis and elongation. Malonyl-CoA decarboxylase (MLYCD, E.C.4.1.1.9), a 55-kDa enzyme catalyses the conversion of malonyl-CoA to acetyl-CoA and carbon dioxide, thus providing a route for disposal of malonyl-CoA from mitochondria and peroxisomes, whereas in the cytosol, the malonyl-CoA pool is regulated by the balance of MLYCD and acetyl-CoA carboxylase activities. So far, 34 cases with different MLYCD gene defects comprising point mutations, stop codons, and frameshift mutations have been reported in the literature. Here, we describe the follow-up of a patient affected by malonic aciduria upon neonatal onset. Molecular analysis showed novel homozygous mutations in the MLYCD gene. Our findings expand the number of reported cases and add a novel variant to the repertoire of MLYCD mutations.

Entities:  

Keywords:  Dilated cardiomyopathy; Malonyl CoA decarboxylase deficiency; fatty acid oxidation defect

Year:  2021        PMID: 33745485     DOI: 10.1017/S104795112100113X

Source DB:  PubMed          Journal:  Cardiol Young        ISSN: 1047-9511            Impact factor:   1.093


  1 in total

1.  Heterogenous Clinical Landscape in a Consanguineous Malonic Aciduria Family.

Authors:  Sarah Snanoudj; Stéphanie Torre; Bénédicte Sudrié-Arnaud; Lenaig Abily-Donval; Alice Goldenberg; Gajja S Salomons; Stéphane Marret; Soumeya Bekri; Abdellah Tebani
Journal:  Int J Mol Sci       Date:  2021-11-23       Impact factor: 5.923

  1 in total

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