Literature DB >> 16251896

Genetics of human heterotaxias.

Lirong Zhu1, John W Belmont, Stephanie M Ware.   

Abstract

The past decade has seen remarkable advances in defining the molecular mechanisms underlying formation of the embryonic left right (LR) axis. This information is slowly transforming our understanding of human birth defects that are caused by disturbed LR axis patterning. Reversals, isomerisms, or segmental discordances of thoraco-abdominal organ position, that is, classic heterotaxy, clearly indicate embryonic disruption of normal LR patterning. Other isolated birth defects, particularly cardiovascular malformations, may be caused by deficiencies in the same pathways. Here, we review the distinctive clinical features of human heterotaxias and try to summarize the known connections between them and the corresponding developmental pathways.

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Year:  2006        PMID: 16251896     DOI: 10.1038/sj.ejhg.5201506

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  47 in total

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7.  New Genetic Insights into Congenital Heart Disease.

Authors:  Stephanie M Ware; John Lynn Jefferies
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Journal:  Am J Med Genet A       Date:  2014-08-06       Impact factor: 2.802

9.  Genetics of congenital heart disease.

Authors:  Ashleigh A Richards; Vidu Garg
Journal:  Curr Cardiol Rev       Date:  2010-05

10.  Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.

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Journal:  Chest       Date:  2014-11       Impact factor: 9.410

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