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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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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. |
format | Online Article Text |
id | pubmed-3762055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT dharmrajmeena sirenomeliaararecaseoffoetalcongenitalanomaly AT gaursumitra sirenomeliaararecaseoffoetalcongenitalanomaly |