Next article Search Articles Instructions for authors  Access Statistics | Citation Manager  
IMAGES  

 Article Access Statistics
    Viewed1978    
    Printed41    
    Emailed0    
    PDF Downloaded96    
    Comments [Add]    

Recommend this journal


Click on image for details.

 Anomalous origin of the left brachiocephalic artery in the right aortic arch: Is there a method to the madness?

Mani Ram Krishna1, Ganesh Kumar Gnanappa1, Rachel Fitzpatrick2, Julian Ayer1, David Winlaw3
1 Department of Pediatric Cardiology, The Children's Hospital at Westmead, Westmead, NSW, Australia
2 Department of Radiology, The Children's Hospital at Westmead, Westmead, NSW, Australia
3 Department of Pediatric Cardiothoracic Surgery, The Children's Hospital at Westmead, Westmead, NSW, Australia

Correspondence Address:
Mani Ram Krishna
The Heart Centre for Children, The Children's Hospital at Westmead, Locked Bag 4001, Westmead, NSW 2145
Australia
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.APC_16_17

Rights and Permissions

Year : 2017  |  Volume : 10  |  Issue : 3  |  Page : 301-303

 
SEARCH
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles

  Article in PDF (626 KB)
Email article
Print Article
Add to My List
The anomalous origin of the left brachiocephalic artery in a right sided aortic arch is a rare vascular ring which might lead to esophageal compression. The exact embryological origin of this anomaly is still widely debated. We present an infant who presented with esophageal compression symptoms and review the various hypotheses about the embryological origin of this anomaly.






[FULL TEXT] [PDF]*
 

 

 Whats new | Sitemap | Feedback | Copyright and Disclaimer
 © 2008 Annals of Pediatric Cardiology | Published by Wolters Kluwer - Medknow
 Online since 20th April, 2008

 

 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 
 
 Reader Comments
 Email Alert *
  *
 * Requires registration (Free)
 
 IMAGES
 



Mani Ram Krishna1, Ganesh Kumar Gnanappa1, Rachel Fitzpatrick2, Julian Ayer1, David Winlaw3
1 Department of Pediatric Cardiology, The Children's Hospital at Westmead, Westmead, NSW, Australia
2 Department of Radiology, The Children's Hospital at Westmead, Westmead, NSW, Australia
3 Department of Pediatric Cardiothoracic Surgery, The Children's Hospital at Westmead, Westmead, NSW, Australia

Correspondence Address:
Mani Ram Krishna
The Heart Centre for Children, The Children's Hospital at Westmead, Locked Bag 4001, Westmead, NSW 2145
Australia
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.APC_16_17

Rights and Permissions

The anomalous origin of the left brachiocephalic artery in a right sided aortic arch is a rare vascular ring which might lead to esophageal compression. The exact embryological origin of this anomaly is still widely debated. We present an infant who presented with esophageal compression symptoms and review the various hypotheses about the embryological origin of this anomaly.






[FULL TEXT] [PDF]*


        
Print this article     Email this article  

 Whats new | Sitemap | Feedback | Copyright and Disclaimer
 © 2008 Annals of Pediatric Cardiology | Published by Wolters Kluwer - Medknow
 Online since 20th April, 2008