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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2013
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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. |
format | Online Article Text |
id | pubmed-3775145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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