An operated case of Holt-Oram syndrome with autosomal dominant inheritance

Z. Czakó, A. Gömöry, P. Homolay, S. Bacsa, S. Kiss, F. Móricz, F. Fülöp, Z. Papp

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

This report is concerned with a patient successfully operated for Holt-Oram syndrome. The disorder is inherited dominantly with complete penetrance and variable expressivity. It is pointed out that in cases of congenital heart disease familial cumulation must be borne in mind which can easily be verified by pedigree investigation. After demonstrating autosomal dominant inheritance, suitable inferences must be drawn for genetic counseling. Attention is drawn to the heart-surgical significance of the rhythm disorders so often associated with the syndrome.

Original languageEnglish
Pages (from-to)60-67
Number of pages8
JournalBasic research in cardiology
Volume71
Issue number1
DOIs
Publication statusPublished - Jan 1 1976

    Fingerprint

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

Cite this

Czakó, Z., Gömöry, A., Homolay, P., Bacsa, S., Kiss, S., Móricz, F., Fülöp, F., & Papp, Z. (1976). An operated case of Holt-Oram syndrome with autosomal dominant inheritance. Basic research in cardiology, 71(1), 60-67. https://doi.org/10.1007/BF01907783