Literature DB >> 668753

The recurrence risk in congenital heart disease.

A Sanchez-Cascos.   

Abstract

We have studied 1148 'isolated" cases of congenital heart disease, taken from a general series of 1255 cases. The recurrence risk ranged from 0.9% for relatives of male cases of VSD and for female cases of aortic stenosis to 10.5% for relatives of female cases of atrioventricularis communis; mean value 2.5%. Heritability ranged from 50% to 95%, mean 65%. Full concordance was more frequent in 1st-degree relatives of Fallot's tetralogy patients, while discordance was common in more distant relatives. We propose a hypothesis of several overlapping polygenic systems for the causation of CHD.

Entities:  

Mesh:

Year:  1978        PMID: 668753

Source DB:  PubMed          Journal:  Eur J Cardiol        ISSN: 0301-4711


  11 in total

1.  Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion.

Authors:  M C Digilio; B Marino; A Giannotti; A Toscano; B Dallapiccola
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

2.  Congenital heart defects--the risks to offspring.

Authors:  J Burn
Journal:  Arch Dis Child       Date:  1983-12       Impact factor: 3.791

Review 3.  Familial recurrence of congenital heart disease: an overview and review of the literature.

Authors:  Giulio Calcagni; M Cristina Digilio; Anna Sarkozy; Bruno Dallapiccola; Bruno Marino
Journal:  Eur J Pediatr       Date:  2006-11-08       Impact factor: 3.183

Review 4.  Familial atrioventricular septal defect: possible genetic mechanisms.

Authors:  A Kumar; C A Williams; B E Victorica
Journal:  Br Heart J       Date:  1994-01

5.  A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic development: studies in the CTD line of keeshond dogs.

Authors:  D F Patterson; T Pexieder; W R Schnarr; T Navratil; R Alaili
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

6.  A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.

Authors:  L Wilson; A Curtis; J R Korenberg; R D Schipper; L Allan; G Chenevix-Trench; A Stephenson; J Goodship; J Burn
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

7.  Genetic study of congenital heart defects in Northern Ireland (1974-1978).

Authors:  E J Hanna; N C Nevin; J Nelson
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

8.  Etiologic heterogeneity in the familial aggregation of congenital cardiovascular malformations.

Authors:  N E Maestri; T H Beaty; J A Boughman
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

Review 9.  Genetic Etiology of Left-Sided Obstructive Heart Lesions: A Story in Development.

Authors:  Lauren E Parker; Andrew P Landstrom
Journal:  J Am Heart Assoc       Date:  2021-01-12       Impact factor: 6.106

Review 10.  Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

Authors:  Paolo Versacci; Flaminia Pugnaloni; Maria Cristina Digilio; Carolina Putotto; Marta Unolt; Giulio Calcagni; Anwar Baban; Bruno Marino
Journal:  J Cardiovasc Dev Dis       Date:  2018-05-02
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