Literature DB >> 3812559

Familial situs inversus and congenital heart defects.

J Zlotogora, M S Schimmel, Y Glaser.   

Abstract

The midline is a major determinant in the lateral symmetry of the embryo and represents a developmental field which, if defective, may lead to an abnormal situs determination. A family in which four out of seven children had situs inversus and/or congenital heart defects is presented. This report confirms the autosomal recessive inheritance of this developmental field defect.

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Year:  1987        PMID: 3812559     DOI: 10.1002/ajmg.1320260126

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 in total

1.  Complete situs inversus and broad thumbs and big toes with postaxial polydactyly.

Authors:  A E Czeizel; P Göblyös
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

Review 2.  Defects in the determination of left-right asymmetry.

Authors:  M P Splitt; J Burn; J Goodship
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

3.  Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies.

Authors:  Lijiang Ma; Elif Seda Selamet Tierney; Teresa Lee; Patricia Lanzano; Wendy K Chung
Journal:  Cardiol Young       Date:  2011-08-25       Impact factor: 1.093

4.  Rare copy number variants in patients with congenital conotruncal heart defects.

Authors:  Hongbo M Xie; Petra Werner; Dwight Stambolian; Joan E Bailey-Wilson; Hakon Hakonarson; Peter S White; Deanne M Taylor; Elizabeth Goldmuntz
Journal:  Birth Defects Res       Date:  2017-02-13       Impact factor: 2.344

5.  Asplenia syndrome and isolated total anomalous pulmonary venous connection in siblings.

Authors:  K Devriendt; A Casaer; A Van Cauter; F de Zegher; M Dumoulin; M Gewillig; H Devlieger
Journal:  Eur J Pediatr       Date:  1994-10       Impact factor: 3.183

  5 in total

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