Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-26T21:12:54.265Z Has data issue: false hasContentIssue false
  • English
  • Français

Double aortic arch in a patient with Fallot's tetralogy

Published online by Cambridge University Press:  14 April 2005

Mathias Emmel ,
Beate Schmidt  and
Sabine Schickendantz
Mathias Emmel
Affiliation:
Department of Paediatric Cardiology, University of Cologne, Cologne, Germany
Beate Schmidt
Affiliation:
Department of Paediatric Cardiology, University of Cologne, Cologne, Germany
Sabine Schickendantz
Affiliation:
Department of Paediatric Cardiology, University of Cologne, Cologne, Germany
Get access Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. Please use the Get access link above for information on how to access this content.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'

Keywords

Vascular ringcyanotic congenital heart diseasemicrodeletion 22q11
Type
Images in Congenital Heart Disease
Information
Cardiology in the Young , Volume 15 , Issue 1 , January 2005 , pp. 52 - 53
Copyright
2005 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

McElhinney DB, Clark BJ, Weinberg PM, et al. Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching. J Am Coll Cardiol 2001; 37: 2114–2119.Google Scholar

Emmel et al video clips

Supplementary Movie

Download Emmel et al video clips(Video)
Video 827.9 KB

Emmel et al video clips

Supplementary Movie

Download Emmel et al video clips(Video)
Video 910.8 KB