European Heart Journal Advance Access originally published online on October 25, 2007
European Heart Journal 2007 28(22):2701-2702; doi:10.1093/eurheartj/ehm479
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Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2007. For permissions please email: journals.permissions@oxfordjournals.org
Catch me if you can: tracking down the genetic origins of congenital heart disease
1 Medical Genetics Division, Sainte Justine Hospital, University of Montreal, Montreal, Québec, Canada
2 Service of Cardiology, Sainte Justine Hospital, University of Montreal, Montreal, Québec, Canada
* Corresponding author. Tel: +1 514 345 4931 ext 3244; fax: +1 514 345 4896. E-mail address: gregor.andelfinger@umontreal.ca
This editorial refers to Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients by B. Thienpont et al., on page 2778
Footnotes
The opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology.
| The first 10% of the full text of this article appears below. |
Congenital heart disease (CHD) is the major cause of death in infants under 1 year of age. CHD kills more children than cancer and accounts for 25% of all birth defects, the single largest category of malformations.1 One newborn in 100 has CHD, and 1 newborn in 1000 will need surgery for CHD. Despite the impressive progress which has been made in deciphering the molecular events governing cardiogenesis, only a minority of heart defects are amenable to routine genetic diagnosis at the present time. Thus, the mechanism of disease remains
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- Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients
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EHJ 2007 28: 2778-2784.[Abstract] [Full Text]