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Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly

A baby with the complete form of pentalogy of Cantrell was delivered at 33 weeks of gestation. The hallmark of this syndrome is ectopia cordis (EC) with omphalocele. Even though a fetal diagnosis was made at 14 weeks, parents have decided to continue with the pregnancy. Early antenatal ultrasonograp...

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Detalles Bibliográficos
Autores principales: Chandran, Suresh, Ari, Dinesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775145/
https://www.ncbi.nlm.nih.gov/pubmed/24049753
http://dx.doi.org/10.4103/2249-4847.116410
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author Chandran, Suresh
Ari, Dinesh
author_facet Chandran, Suresh
Ari, Dinesh
author_sort Chandran, Suresh
collection PubMed
description A baby with the complete form of pentalogy of Cantrell was delivered at 33 weeks of gestation. The hallmark of this syndrome is ectopia cordis (EC) with omphalocele. Even though a fetal diagnosis was made at 14 weeks, parents have decided to continue with the pregnancy. Early antenatal ultrasonographic diagnosis is essential as survival depends mostly on the EC, associated cardiac anomalies and degree of thoraco-abdominal defect. Fetal diagnosis of this lethal anomaly before viability gives the parents an option of termination.
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spelling pubmed-37751452013-09-18 Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly Chandran, Suresh Ari, Dinesh J Clin Neonatol Case Report A baby with the complete form of pentalogy of Cantrell was delivered at 33 weeks of gestation. The hallmark of this syndrome is ectopia cordis (EC) with omphalocele. Even though a fetal diagnosis was made at 14 weeks, parents have decided to continue with the pregnancy. Early antenatal ultrasonographic diagnosis is essential as survival depends mostly on the EC, associated cardiac anomalies and degree of thoraco-abdominal defect. Fetal diagnosis of this lethal anomaly before viability gives the parents an option of termination. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3775145/ /pubmed/24049753 http://dx.doi.org/10.4103/2249-4847.116410 Text en Copyright: © Journal of Clinical Neonatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chandran, Suresh
Ari, Dinesh
Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly
title Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly
title_full Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly
title_fullStr Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly
title_full_unstemmed Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly
title_short Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly
title_sort pentalogy of cantrell: an extremely rare congenital anomaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775145/
https://www.ncbi.nlm.nih.gov/pubmed/24049753
http://dx.doi.org/10.4103/2249-4847.116410
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