Hypertrophic cardiomyopathy associated with congenital deaf-mutism

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

A family is presented in which there is a high incidence of hypertrophic cardiomyopathy and congenital deaf-mutism. The two abnormalities occurred together in 2 cases, and the syndrome was strongly suspected in a third individual. Hypertrophic cardiomyopathy without deaf-mutism was observed in a further 2 cases. Hypertrophic cardiomyopathy is inherited by an autosomal dominant mode; that occurring together with deaf-mutism is also probably inherited dominantly.

Original languageEnglish
Pages (from-to)528-534
Number of pages7
JournalEuropean Heart Journal
Volume8
Issue number5
Publication statusPublished - May 1987

Fingerprint

Cardiomyopathy
Hypertrophic Cardiomyopathy
Deafness
Incidence
Hypertrophic cardiomyopathy

Keywords

  • Congenital deaf-mutism
  • Enhanced familial incidence
  • Hypertrophic cardiomyopathy
  • Mode of inheritance

ASJC Scopus subject areas

  • Statistics, Probability and Uncertainty
  • Applied Mathematics
  • Physiology (medical)
  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Hypertrophic cardiomyopathy associated with congenital deaf-mutism. / Csanády, M.; Högye, M.; Forster, T.

In: European Heart Journal, Vol. 8, No. 5, 05.1987, p. 528-534.

Research output: Contribution to journalArticle

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