Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: Shrestha, Nischal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of the Nepal Medical Association 2022
Materias:
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
_version_ 1784727970879897600
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
work_keys_str_mv AT shresthanischal ababybornwithectopiacordisomphalocelecleftlipsandpalateacasereport
AT shresthanischal babybornwithectopiacordisomphalocelecleftlipsandpalateacasereport