Defining the molecular genetic basis of idiopathic dilated cardiomyopathy

Timothy Mark Olson, Mark T. Keating

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Dilated cardiomyopathy (DCM) is a significant health care problem. The etiology is idiopathic in approximately half of the patients. Recognition that 20%-25% of idiopathic DCM cases are familial has advanced the hypothesis that single gene defects are important in the disease's pathogenesis. General linkage analyses in rare, large DCM families have determined the chromosome location of five idiopathic DCM genes. Candidate-gene mutational analyses in more typical, small pedigrees represent an alternative strategy for DCM gene identification. Human molecular genetics will play a fundamental role in defining pathogenic mechanisms for DCM with the prospect of new, molecular- based diagnostic and therapeutic approaches.

Original languageEnglish (US)
Pages (from-to)60-63
Number of pages4
JournalTrends in Cardiovascular Medicine
Volume7
Issue number2
DOIs
StatePublished - Feb 1997
Externally publishedYes

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Dilated Cardiomyopathy
Molecular Biology
Inborn Genetic Diseases
Molecular Pathology
Medical Genetics
Genetic Association Studies
Pedigree
Genes
Chromosomes
Delivery of Health Care

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

Defining the molecular genetic basis of idiopathic dilated cardiomyopathy. / Olson, Timothy Mark; Keating, Mark T.

In: Trends in Cardiovascular Medicine, Vol. 7, No. 2, 02.1997, p. 60-63.

Research output: Contribution to journalArticle

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