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Mermaid Syndrome: A Case Report in Mauritius

Sirenomelia is a rare congenital malformation that results in the fusion of the lower limbs together with multiple visceral anomalies. We report a case of sirenomelia observed in Mauritius and the different findings seen in the baby. The baby had fused lower extremities and bony structures for each...

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Autores principales: Ramphul, Kamleshun, Mejias, Stephanie G, Ramphul-Sicharam, Yogeshwaree
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910014/
https://www.ncbi.nlm.nih.gov/pubmed/29686952
http://dx.doi.org/10.7759/cureus.2210
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author Ramphul, Kamleshun
Mejias, Stephanie G
Ramphul-Sicharam, Yogeshwaree
author_facet Ramphul, Kamleshun
Mejias, Stephanie G
Ramphul-Sicharam, Yogeshwaree
author_sort Ramphul, Kamleshun
collection PubMed
description Sirenomelia is a rare congenital malformation that results in the fusion of the lower limbs together with multiple visceral anomalies. We report a case of sirenomelia observed in Mauritius and the different findings seen in the baby. The baby had fused lower extremities and bony structures for each leg were present. The umbilical cord consisted of a single artery and one vein. The external genitalia was absent and an imperforate anus was also seen. An x-ray revealed poorly expanded lungs and two distinct sets of femur and tibia were seen on imaging. However, a fused fibula and a fused talus were also noted. Multiple theories have been suggested for the pathogenesis of this condition, and despite recent progress in pathology, this condition remains debated.
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spelling pubmed-59100142018-04-23 Mermaid Syndrome: A Case Report in Mauritius Ramphul, Kamleshun Mejias, Stephanie G Ramphul-Sicharam, Yogeshwaree Cureus Pediatrics Sirenomelia is a rare congenital malformation that results in the fusion of the lower limbs together with multiple visceral anomalies. We report a case of sirenomelia observed in Mauritius and the different findings seen in the baby. The baby had fused lower extremities and bony structures for each leg were present. The umbilical cord consisted of a single artery and one vein. The external genitalia was absent and an imperforate anus was also seen. An x-ray revealed poorly expanded lungs and two distinct sets of femur and tibia were seen on imaging. However, a fused fibula and a fused talus were also noted. Multiple theories have been suggested for the pathogenesis of this condition, and despite recent progress in pathology, this condition remains debated. Cureus 2018-02-20 /pmc/articles/PMC5910014/ /pubmed/29686952 http://dx.doi.org/10.7759/cureus.2210 Text en Copyright © 2018, Ramphul et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pediatrics
Ramphul, Kamleshun
Mejias, Stephanie G
Ramphul-Sicharam, Yogeshwaree
Mermaid Syndrome: A Case Report in Mauritius
title Mermaid Syndrome: A Case Report in Mauritius
title_full Mermaid Syndrome: A Case Report in Mauritius
title_fullStr Mermaid Syndrome: A Case Report in Mauritius
title_full_unstemmed Mermaid Syndrome: A Case Report in Mauritius
title_short Mermaid Syndrome: A Case Report in Mauritius
title_sort mermaid syndrome: a case report in mauritius
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910014/
https://www.ncbi.nlm.nih.gov/pubmed/29686952
http://dx.doi.org/10.7759/cureus.2210
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