Literature DB >> 4019923

A possible increase in the incidence of congenital heart defects among the offspring of affected parents.

V Rose, R J Gold, G Lindsay, M Allen.   

Abstract

The incidence of congenital heart disease in the children of 219 probands was determined. Each of these probands had one of four selected defects: atrial septal defect, coarctation of the aorta, aortic valve stenosis or complex dextrocardia. Of their children, 8.8% had substantial congenital cardiac defects. This is a much higher incidence than that reported in most comparable studies. The difference is highly significant statistically and therefore is likely to be genuine. The cause of the high recurrence is probably environmental.

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Year:  1985        PMID: 4019923     DOI: 10.1016/s0735-1097(85)80175-3

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  14 in total

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Authors:  J Insley
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3.  Prevalence of congenital heart disease.

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Review 4.  Genetic counseling for congenital heart disease: new approaches for a new decade.

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5.  Risk of congenital heart disease in relatives of probands with conotruncal cardiac defects: an evaluation of 1,620 families.

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6.  History of Our Understanding of the Causes of Congenital Heart Disease.

Authors:  Bruce D Gelb
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7.  Outcome of pregnancy in women with congenital shunt lesions.

Authors:  M Zuber; N Gautschi; E Oechslin; V Widmer; W Kiowski; R Jenni
Journal:  Heart       Date:  1999-03       Impact factor: 5.994

8.  Improving the effectiveness of routine prenatal screening for major congenital heart defects.

Authors:  J S Carvalho; E Mavrides; E A Shinebourne; S Campbell; B Thilaganathan
Journal:  Heart       Date:  2002-10       Impact factor: 5.994

9.  Preconceptual Folic Acid Use and Recurrence Risk Counseling for Congenital Heart Disease.

Authors:  Shabnam Peyvandi; Jack Rychik; Xuemei Zhang; Judy A Shea; Elizabeth Goldmuntz
Journal:  Congenit Heart Dis       Date:  2014-07-24       Impact factor: 2.007

10.  Identification of two novel mutations of the HOMEZ gene in Chinese patients with isolated ventricular septal defect.

Authors:  Chao Xuan; Ke-Gang Jia; Bin-Bin Wang; Xiao-Yan Bai; Ge Gao; Qin Yang; Xiu-Li Wang; Xiao-Cheng Liu; Xu Ma; Guo-Wei He
Journal:  Genet Test Mol Biomarkers       Date:  2013-04-10
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