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Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity

Embryologically, the common arterial trunk (CAT) is due to the failure of septation by the major outflow cushions. This invariably leads to the presence of an associated large juxta-arterial ventricular septal defect. Overriding of the ventricular septum leads to its biventricular origin in more tha...

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Autores principales: Chikkagoudar, Kalyanraddi, Gupta, Palak, Koneti, Nageswara Rao, Dash, Tapan K, Doraiswamy, Vinoth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331841/
https://www.ncbi.nlm.nih.gov/pubmed/32641891
http://dx.doi.org/10.4103/apc.APC_48_19
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author Chikkagoudar, Kalyanraddi
Gupta, Palak
Koneti, Nageswara Rao
Dash, Tapan K
Doraiswamy, Vinoth
author_facet Chikkagoudar, Kalyanraddi
Gupta, Palak
Koneti, Nageswara Rao
Dash, Tapan K
Doraiswamy, Vinoth
author_sort Chikkagoudar, Kalyanraddi
collection PubMed
description Embryologically, the common arterial trunk (CAT) is due to the failure of septation by the major outflow cushions. This invariably leads to the presence of an associated large juxta-arterial ventricular septal defect. Overriding of the ventricular septum leads to its biventricular origin in more than 2/3(rd) of cases. Uncommonly, CAT may be associated with an intact ventricular septum (IVS) and univentricular origin. We describe an infant with CAT, intact IVS, hypoplastic right ventricle, and Ebstein's anomaly of the tricuspid valve who presented to us and palliated successfully. The embryological mechanisms are discussed in this report.
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spelling pubmed-73318412020-07-07 Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity Chikkagoudar, Kalyanraddi Gupta, Palak Koneti, Nageswara Rao Dash, Tapan K Doraiswamy, Vinoth Ann Pediatr Cardiol Case Report Embryologically, the common arterial trunk (CAT) is due to the failure of septation by the major outflow cushions. This invariably leads to the presence of an associated large juxta-arterial ventricular septal defect. Overriding of the ventricular septum leads to its biventricular origin in more than 2/3(rd) of cases. Uncommonly, CAT may be associated with an intact ventricular septum (IVS) and univentricular origin. We describe an infant with CAT, intact IVS, hypoplastic right ventricle, and Ebstein's anomaly of the tricuspid valve who presented to us and palliated successfully. The embryological mechanisms are discussed in this report. Wolters Kluwer - Medknow 2020 2020-04-13 /pmc/articles/PMC7331841/ /pubmed/32641891 http://dx.doi.org/10.4103/apc.APC_48_19 Text en Copyright: © 2020 Annals of Pediatric Cardiology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Chikkagoudar, Kalyanraddi
Gupta, Palak
Koneti, Nageswara Rao
Dash, Tapan K
Doraiswamy, Vinoth
Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity
title Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity
title_full Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity
title_fullStr Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity
title_full_unstemmed Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity
title_short Common arterial trunk with intact septum and hypoplastic right ventricle: An uncommon embryological entity
title_sort common arterial trunk with intact septum and hypoplastic right ventricle: an uncommon embryological entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331841/
https://www.ncbi.nlm.nih.gov/pubmed/32641891
http://dx.doi.org/10.4103/apc.APC_48_19
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