Risk of congenital heart defects in relatives of patients with atrioventricular canal

Am J Dis Child. 1993 Dec;147(12):1295-7. doi: 10.1001/archpedi.1993.02160360037013.

Abstract

Objective: To investigate the overall occurrence of congenital heart disease in 103 pedigrees with a proband affected with atrioventricular canal.

Design: Family study of patient series.

Setting: Department of Pediatric Cardiology, Bambino Gesu' Hospital, Rome, Italy.

Participants: One hundred three consecutive patients with atrioventricular canal and normal karyotype and their first- and second-degree relatives.

Interventions: None.

Measurements/main results: In 12 pedigrees (11.7%), one or more relatives had concordant or discordant congenital heart disease. Congenital heart disease occurred in four (1.9%) of the 206 parents of probands, in four (3.6%) of the 111 siblings, and in five (0.8%) of the 644 uncles or aunts. None of the grandparents had congenital heart disease. Atrioventricular canal affected several family members in five pedigrees.

Conclusions: Familial aggregation of atrioventricular canal in several pedigrees requires careful collection of family histories, accurate cardiologic evaluation of the first- and second-degree relatives of the probands, and fetal echocardiography in all pregnant women in at-risk families.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Endocardial Cushion Defects / genetics*
  • Female
  • Heart Defects, Congenital / genetics*
  • Humans
  • Infant
  • Male
  • Pedigree
  • Risk Factors