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A Baby Born with Ectopia Cordis, Omphalocele, Cleft Lips and Palate: A Case Report
Ectopia cordis is a rare congenital defect with the prevalence of 5 to 8 per million live births. Here we report a rare case of preterm female live birth with ectopia cordis associated with omphalocele, cleft lip, and palate. In this case, 14+ weeks ultrasound did not show any fetal abnormalities an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Journal of the Nepal Medical Association
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200009/ https://www.ncbi.nlm.nih.gov/pubmed/35210636 http://dx.doi.org/10.31729/jnma.7153 |
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author | Shrestha, Nischal |
author_facet | Shrestha, Nischal |
author_sort | Shrestha, Nischal |
collection | PubMed |
description | Ectopia cordis is a rare congenital defect with the prevalence of 5 to 8 per million live births. Here we report a rare case of preterm female live birth with ectopia cordis associated with omphalocele, cleft lip, and palate. In this case, 14+ weeks ultrasound did not show any fetal abnormalities and parents were unaware of the condition until 35+ weeks when ultrasound detected the anomaly a few days before delivery. After delivery, they didn't give consent for further intervention which led to neonatal mortality 3 hours after birth. If the condition was diagnosed in time, an earlier intervention could have been done. |
format | Online Article Text |
id | pubmed-9200009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Journal of the Nepal Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-92000092022-06-21 A Baby Born with Ectopia Cordis, Omphalocele, Cleft Lips and Palate: A Case Report Shrestha, Nischal JNMA J Nepal Med Assoc Case Report Ectopia cordis is a rare congenital defect with the prevalence of 5 to 8 per million live births. Here we report a rare case of preterm female live birth with ectopia cordis associated with omphalocele, cleft lip, and palate. In this case, 14+ weeks ultrasound did not show any fetal abnormalities and parents were unaware of the condition until 35+ weeks when ultrasound detected the anomaly a few days before delivery. After delivery, they didn't give consent for further intervention which led to neonatal mortality 3 hours after birth. If the condition was diagnosed in time, an earlier intervention could have been done. Journal of the Nepal Medical Association 2022-02 2022-02-28 /pmc/articles/PMC9200009/ /pubmed/35210636 http://dx.doi.org/10.31729/jnma.7153 Text en © The Author(s) 2018. https://creativecommons.org/licenses/by/4.0/This is an Open-Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Shrestha, Nischal A Baby Born with Ectopia Cordis, Omphalocele, Cleft Lips and Palate: A Case Report |
title | A Baby Born with Ectopia Cordis, Omphalocele, Cleft Lips and Palate: A Case Report |
title_full | A Baby Born with Ectopia Cordis, Omphalocele, Cleft Lips and Palate: A Case Report |
title_fullStr | A Baby Born with Ectopia Cordis, Omphalocele, Cleft Lips and Palate: A Case Report |
title_full_unstemmed | A Baby Born with Ectopia Cordis, Omphalocele, Cleft Lips and Palate: A Case Report |
title_short | A Baby Born with Ectopia Cordis, Omphalocele, Cleft Lips and Palate: A Case Report |
title_sort | baby born with ectopia cordis, omphalocele, cleft lips and palate: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200009/ https://www.ncbi.nlm.nih.gov/pubmed/35210636 http://dx.doi.org/10.31729/jnma.7153 |
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