Literature DB >> 9568229

Hypertrophic cardiomyopathy with mitochondrial DNA depletion and respiratory enzyme defects.

J Marin-Garcia1, R Ananthakrishnan, M J Goldenthal.   

Abstract

We report the case of a child with severe hypertrophic cardiomyopathy, with decreased activity levels of cardiac mitochondrial respiratory complex I and III, and with a pronounced reduction in cardiac mitochondrial DNA copy number level. Mitochondrial DNA depletion has not been previously reported in hypertrophic cardiomyopathy and it may play a role in its pathogenesis.

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Year:  1998        PMID: 9568229     DOI: 10.1007/s002469900303

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  3 in total

Review 1.  Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.

Authors:  A Brega; J Narula; E Arbustini
Journal:  J Nucl Cardiol       Date:  2001 Jan-Feb       Impact factor: 5.952

2.  Infantile mitochondrial DNA depletion syndrome associated with methylmalonic aciduria and 3-methylcrotonyl-CoA and propionyl-CoA carboxylase deficiencies in two unrelated patients: a new phenotype of mtDNA depletion syndrome.

Authors:  S Yano; L Li; T P Le; K Moseley; A Guedalia; J Lee; I Gonzalez; R G Boles
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 3.  Approach to congenital heart disease in the neonate.

Authors:  Usha S Krishnan
Journal:  Indian J Pediatr       Date:  2002-06       Impact factor: 1.967

  3 in total

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