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Isolation of the left subclavian artery in an infant with tetralogy of Fallot, right aortic arch and DiGeorge syndrome. Echocardiographic diagnostic case study Cover

Isolation of the left subclavian artery in an infant with tetralogy of Fallot, right aortic arch and DiGeorge syndrome. Echocardiographic diagnostic case study

Journal of Ultrasonography
Volume 19 (2019): Issue 76 (March 2019)
By: Maciej A. Karolczak,  Wojciech Mądry and  Darren James Grégoire  
Open Access
|Apr 2019

Authors

Maciej A. Karolczak

maciej.karolczak@spdsk.edu.pl

Department of Cardiac and General Pediatric Surgery, Medical University of Warsaw, Warsaw, Poland

Wojciech Mądry

Department of Cardiac and General Pediatric Surgery, Medical University of Warsaw, Warsaw, Poland

Darren James Grégoire

Department of Cardiac and General Pediatric Surgery, Medical University of Warsaw, Warsaw, Poland
DOI: https://doi.org/10.15557/jou.2019.0010 | Journal eISSN: 2451-070X | Journal ISSN: 2084-8404
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Language: English
Page range: 66 - 70
Submitted on: Nov 4, 2018
Accepted on: Jan 22, 2019
Published on: Apr 30, 2019
Published by: MEDICAL COMMUNICATIONS Sp. z o.o.
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Keywords:
isolated left subclavian artery,
tetralogy of Fallot,
DiGeorge syndrome,
right aortic arch
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2019 Maciej A. Karolczak, Wojciech Mądry, Darren James Grégoire, published by MEDICAL COMMUNICATIONS Sp. z o.o.
This work is licensed under the Creative Commons Attribution 4.0 License.

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