Literature DB >> 17091259

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

Giulio Calcagni1, M Cristina Digilio, Anna Sarkozy, Bruno Dallapiccola, Bruno Marino.   

Abstract

Familial recurrence is one of the classic patterns for the clinical presentation of congenital heart disease (CHD). In recent years, many groups studied empiric recurrence risk in these heart defects, and the aim of this review was to analyse the patterns of inheritance detected in different types of CHD, including atrioventricular canal defect, tetralogy of Fallot, transposition of the great arteries, left-sided obstructions and atrial septal defect. These studies may influence clinical practise guidelines through accurate genetic counselling, but also, they may have important implications in the knowledge of genetic and pathogenetic mechanisms of CHD.

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Year:  2006        PMID: 17091259     DOI: 10.1007/s00431-006-0295-9

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  47 in total

1.  Familial Tetralogy of Fallot caused by mutation in the jagged1 gene.

Authors:  Z A Eldadah; A Hamosh; N J Biery; R A Montgomery; M Duke; R Elkins; H C Dietz
Journal:  Hum Mol Genet       Date:  2001-01-15       Impact factor: 6.150

Review 2.  Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction.

Authors:  J J Nora
Journal:  Circulation       Date:  1968-09       Impact factor: 29.690

3.  Familial clustering of atrioventricular canal defects.

Authors:  S N Tennant; J W Hammon; H W Bender; T P Graham; R K Primm
Journal:  Am Heart J       Date:  1984-07       Impact factor: 4.749

4.  Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence.

Authors:  M C Digilio; B Casey; A Toscano; R Calabrò; G Pacileo; M Marasini; E Banaudi; A Giannotti; B Dallapiccola; B Marino
Journal:  Circulation       Date:  2001-12-04       Impact factor: 29.690

5.  Familial recurrence of heart defects in subjects with congenitally corrected transposition of the great arteries.

Authors:  Gerardo Piacentini; M Cristina Digilio; Rossella Capolino; Andrea De Zorzi; Alessandra Toscano; Anna Sarkozy; Rita D'Agostino; Maurizio Marasini; M Giovanna Russo; Bruno Dallapiccola; Bruno Marino
Journal:  Am J Med Genet A       Date:  2005-08-30       Impact factor: 2.802

6.  Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis.

Authors:  V C Sheffield; M E Pierpont; D Nishimura; J S Beck; T L Burns; M A Berg; E M Stone; S R Patil; R M Lauer
Journal:  Hum Mol Genet       Date:  1997-01       Impact factor: 6.150

7.  Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.

Authors:  Kim L McBride; Ricardo Pignatelli; Mark Lewin; Trang Ho; Susan Fernbach; Andres Menesses; Wilbur Lam; Suzanne M Leal; Norman Kaplan; Paul Schliekelman; Jeffrey A Towbin; John W Belmont
Journal:  Am J Med Genet A       Date:  2005-04-15       Impact factor: 2.802

Review 8.  Familial atrioventricular septal defect: possible genetic mechanisms.

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

9.  GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.

Authors:  Vidu Garg; Irfan S Kathiriya; Robert Barnes; Marie K Schluterman; Isabelle N King; Cheryl A Butler; Caryn R Rothrock; Reenu S Eapen; Kayoko Hirayama-Yamada; Kunitaka Joo; Rumiko Matsuoka; Jonathan C Cohen; Deepak Srivastava
Journal:  Nature       Date:  2003-07-06       Impact factor: 49.962

10.  Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects.

Authors:  D W Benson; A Sharkey; D Fatkin; P Lang; C T Basson; B McDonough; A W Strauss; J G Seidman; C E Seidman
Journal:  Circulation       Date:  1998-05-26       Impact factor: 29.690

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  25 in total

Review 1.  The changing epidemiology of congenital heart disease.

Authors:  Teun van der Bom; A Carla Zomer; Aeilko H Zwinderman; Folkert J Meijboom; Berto J Bouma; Barbara J M Mulder
Journal:  Nat Rev Cardiol       Date:  2010-11-02       Impact factor: 32.419

Review 2.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

Review 3.  Genetic testing in congenital heart disease: A clinical approach.

Authors:  Marie A Chaix; Gregor Andelfinger; Paul Khairy
Journal:  World J Cardiol       Date:  2016-02-26

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

Authors:  Shabnam Peyvandi; Eitan Ingall; Stacy Woyciechowski; Jennifer Garbarini; Laura E Mitchell; Elizabeth Goldmuntz
Journal:  Am J Med Genet A       Date:  2014-03-26       Impact factor: 2.802

5.  Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography.

Authors:  Fernanda Teixeira da Silva Bellucco; Sintia Iole Nogueira Belangero; Leila Montenegro Silveira Farah; Maria Virgínia Lima Machado; Adriano Pastor Cruz; Lílian Maria Lopes; Marco Antonio Borges Lopes; Marcelo Zugaib; Mirlene Cecília Cernach; Maria Isabel Melaragno
Journal:  Pediatr Cardiol       Date:  2010-09-17       Impact factor: 1.655

Review 6.  Appropriate Use of Genetic Testing in Congenital Heart Disease Patients.

Authors:  Seiji Ito; Kimberly A Chapman; Monisha Kisling; Anitha S John
Journal:  Curr Cardiol Rep       Date:  2017-03       Impact factor: 2.931

7.  Is a shorter atrioventricular septal length an intermediate phenotype in the spectrum of nonsyndromic atrioventricular septal defects?

Authors:  Sonali S Patel; Larry T Mahoney; Trudy L Burns
Journal:  J Am Soc Echocardiogr       Date:  2012-04-25       Impact factor: 5.251

8.  Increased prevalence of cardiovascular defects among 56,709 California twin pairs.

Authors:  J Hardin; S L Carmichael; S Selvin; E J Lammer; G M Shaw
Journal:  Am J Med Genet A       Date:  2009-05       Impact factor: 2.802

9.  Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.

Authors:  Ozanna Burnicka-Turek; Jeffrey D Steimle; Wenhui Huang; Lindsay Felker; Anna Kamp; Junghun Kweon; Michael Peterson; Roger H Reeves; Cheryl L Maslen; Peter J Gruber; Xinan H Yang; Jay Shendure; Ivan P Moskowitz
Journal:  Hum Mol Genet       Date:  2016-06-23       Impact factor: 6.150

10.  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

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