Literature DB >> 19691901

Defects in long chain fatty acid oxidation presenting as severe cardiomyopathy and cardiogenic shock in infancy.

Narendra R Dereddy1, David Kronn, Usha Krishnan.   

Abstract

Inborn errors of fatty acid metabolism are important causes of reversible cardiomyopathy in infancy. Disorders in long chain fatty acid oxidation can lead to cardiomyopathy, as fatty acid beta oxidation is the major source of myocardial energy after birth. We present 2 cases of such disorders with cardiac manifestations during infancy, which responded well to a diet low in long chain fatty acids.

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Year:  2009        PMID: 19691901     DOI: 10.1017/S104795110999134X

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


  3 in total

1.  Cardiac failure in very long chain acyl-CoA dehydrogenase deficiency requiring extracorporeal membrane oxygenation (ECMO) treatment: A case report and review of the literature.

Authors:  Sharon Katz; Yuval Landau; Ben Pode-Shakked; Itai M Pessach; Marina Rubinshtein; Yair Anikster; Yishay Salem; Gideon Paret
Journal:  Mol Genet Metab Rep       Date:  2016-12-08

2.  Defects in Very Long-Chain Fatty Acid Oxidation Presenting as Different Types of Cardiomyopathy.

Authors:  Fariba Alaei; Marjan Shakiba; Hedyeh Saneifard; Kourosh Vahidshahi; Mastaneh Alaei
Journal:  Case Rep Cardiol       Date:  2022-04-28

3.  Treatable massive pericardial effusion and hypertrophic cardiomyopathy in an infant with a novel homozygous ACADVL mutation: A case report.

Authors:  Yoo-Mi Kim; Geena Kim; Hoon Ko; Han-Wook Yoo; Hyoung Doo Lee
Journal:  Medicine (Baltimore)       Date:  2018-05       Impact factor: 1.889

  3 in total

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