Literature DB >> 11162282

Congenital heart malformations: aetiology and associations.

P Brennan1, I D Young.   

Abstract

The causes of congenital heart malformations are complex and include a major contribution by genetic factors. These can be considered under the headings of chromosomal, single gene and multifactorial. Almost any degree of autosomal imbalance, whether a full trisomy or a tiny microdeletion, can cause a cardiac malformation. Recent research has identified several developmental genes which play an important role in cardiac formation: these are discussed with regard to laterality, septation and vascular morphogenesis. Hypothetical 'polygenes', which may contribute to non-syndromal 'multifactorial' cardiac malformations have yet to be identified. Well-known cardiac malformation syndrome associations are described and simple guidelines are presented to help in the assessment and investigation of an affected neonate who has additional multiple dysmorphic features. Copyright 2001 Harcourt Publishers Ltd.

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Year:  2001        PMID: 11162282     DOI: 10.1053/siny.2000.0032

Source DB:  PubMed          Journal:  Semin Neonatol        ISSN: 1084-2756


  7 in total

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Authors:  Maria Romøren; Morten Lindbæk; Hedvig Nordeng
Journal:  Br J Clin Pharmacol       Date:  2012-12       Impact factor: 4.335

3.  Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil.

Authors:  Bruna Lixinski Diniz; Andressa Schneiders Santos; Andressa Barreto Glaeser; Bruna Baierle Guaraná; Cláudia Fernandes Lorea; Juliana Alves Josahkian; Janaína Huber; Rafael Fabiano Machado Rosa; Paulo Ricardo Gazzola Zen
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4.  Spatial patterns of the congenital heart disease prevalence among 0- to 14-year-old children in Sichuan Basin, P. R China, from 2004 to 2009.

Authors:  Li-Guang Ma; Jun Zhao; Zhou-Peng Ren; Yuan-Yuan Wang; Zuo-Qi Peng; Jin-Feng Wang; Xu Ma
Journal:  BMC Public Health       Date:  2014-06-12       Impact factor: 3.295

5.  The role of histone modification and a regulatory single-nucleotide polymorphism (rs2071166) in the Cx43 promoter in patients with TOF.

Authors:  Ruoyi Gu; Jun Xu; Yixiang Lin; Wei Sheng; Duan Ma; Xiaojing Ma; Guoying Huang
Journal:  Sci Rep       Date:  2017-09-05       Impact factor: 4.379

6.  Inhibition of miR-29c promotes proliferation, and inhibits apoptosis and differentiation in P19 embryonic carcinoma cells.

Authors:  Bin Chen; Guixian Song; Ming Liu; Lingmei Qian; Lihua Wang; Haitao Gu; Yahui Shen
Journal:  Mol Med Rep       Date:  2016-01-29       Impact factor: 2.952

7.  Health-related quality of life of mothers of children with congenital heart disease in a sub-Saharan setting: cross-sectional comparative study.

Authors:  Lidia Sileshi; Endale Tefera
Journal:  BMC Res Notes       Date:  2017-10-26
  7 in total

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