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Sirenomelia: A Rare Case of Foetal Congenital Anomaly

Sirenomelia, alternatively known as ‘mermaid syndrome’ is a very rare congenital deformity in which the legs are fused together, giving them the appearance of the tail of a mermaid’. Other birth defects are always associated with sirenomelia, most commonly abnormalities of the kidneys, large intesti...

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Detalles Bibliográficos
Autores principales: Dharmraj, Meena, Gaur, Sumitra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762055/
https://www.ncbi.nlm.nih.gov/pubmed/24027732
http://dx.doi.org/10.4103/2249-4847.106006
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author Dharmraj, Meena
Gaur, Sumitra
author_facet Dharmraj, Meena
Gaur, Sumitra
author_sort Dharmraj, Meena
collection PubMed
description Sirenomelia, alternatively known as ‘mermaid syndrome’ is a very rare congenital deformity in which the legs are fused together, giving them the appearance of the tail of a mermaid’. Other birth defects are always associated with sirenomelia, most commonly abnormalities of the kidneys, large intestines, and genitalia. The present case is a one of sirenomelia associated with an absent right kidney, mild left hydronephrosis, single umbilical artery, and severe oligohydramnios. We discuss the findings, relative to the present literature and related etiopathogenesis.
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spelling pubmed-37620552013-09-11 Sirenomelia: A Rare Case of Foetal Congenital Anomaly Dharmraj, Meena Gaur, Sumitra J Clin Neonatol Case Report Sirenomelia, alternatively known as ‘mermaid syndrome’ is a very rare congenital deformity in which the legs are fused together, giving them the appearance of the tail of a mermaid’. Other birth defects are always associated with sirenomelia, most commonly abnormalities of the kidneys, large intestines, and genitalia. The present case is a one of sirenomelia associated with an absent right kidney, mild left hydronephrosis, single umbilical artery, and severe oligohydramnios. We discuss the findings, relative to the present literature and related etiopathogenesis. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3762055/ /pubmed/24027732 http://dx.doi.org/10.4103/2249-4847.106006 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
Dharmraj, Meena
Gaur, Sumitra
Sirenomelia: A Rare Case of Foetal Congenital Anomaly
title Sirenomelia: A Rare Case of Foetal Congenital Anomaly
title_full Sirenomelia: A Rare Case of Foetal Congenital Anomaly
title_fullStr Sirenomelia: A Rare Case of Foetal Congenital Anomaly
title_full_unstemmed Sirenomelia: A Rare Case of Foetal Congenital Anomaly
title_short Sirenomelia: A Rare Case of Foetal Congenital Anomaly
title_sort sirenomelia: a rare case of foetal congenital anomaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762055/
https://www.ncbi.nlm.nih.gov/pubmed/24027732
http://dx.doi.org/10.4103/2249-4847.106006
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