Hereditary Atrial Septal Defect
- 1 June 1978
- journal article
- research article
- Published by American Medical Association (AMA) in American Journal of Diseases of Children
- Vol. 132 (6) , 600-604
- https://doi.org/10.1001/archpedi.1978.02120310064013
Abstract
• A large pedigree wherein members are predisposed to atrial septal defect (ASD) and associated cardiovascular anomalies has been studied. There were ten direct line relatives with ASD verified by cardiac catheterization and/or surgery and in one case by reliable medical history. The pedigree shows vertical transmission of ASD through four generations. Estimates of the genetic segregation ratio were near 50%, indicating that predisposition to ASD among family members was due to a deleterious autosomal dominant gene. Family members have also manifested other congenital heart anomalies, consistent with pleiotropic effects of the putative gene. Electrocardiograms in six ASD patients revealed an absence of prolonged P-R interval. In the light of prior studies showing prolonged P-R interval in familial ASD, we suggest the existence of at least two distinct hereditary varieties of ASD, one with and one without a prolonged P-R interval. (Am J Dis Child 132:600-604, 1978)This publication has 4 references indexed in Scilit:
- Familial atrial septal defect with prolonged atrioventricular conduction.Circulation, 1976
- INHERITANCE OF ATRIAL SEPTAL DEFECTThe Lancet, 1967
- Spontaneous Functional Closure of Symptomatic Atrial Septal DefectsNew England Journal of Medicine, 1967
- Atrial septal defectThe American Journal of Cardiology, 1962