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Sirenomelia Apus: A Rare Deformity
Sirenomelia also known as the mermaid syndrome, is a rare congenital malformation of uncertain etiology. It is characterized by fusion of the lower limbs and commonly associated with severe urogenital and gastrointestinal malformations. There are approximately 300 cases reported in the literature, 1...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762023/ https://www.ncbi.nlm.nih.gov/pubmed/24027712 http://dx.doi.org/10.4103/2249-4847.101699 |
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author | Kshirsagar, Vinayak Y. Ahmed, Minhajuddin Colaco, Sylvia M. |
author_facet | Kshirsagar, Vinayak Y. Ahmed, Minhajuddin Colaco, Sylvia M. |
author_sort | Kshirsagar, Vinayak Y. |
collection | PubMed |
description | Sirenomelia also known as the mermaid syndrome, is a rare congenital malformation of uncertain etiology. It is characterized by fusion of the lower limbs and commonly associated with severe urogenital and gastrointestinal malformations. There are approximately 300 cases reported in the literature, 15% of which are associated with twinning, most often monozygotic. The syndrome of caudal regression is thought to be the result of injury to the caudal mesoderm early in gestation. |
format | Online Article Text |
id | pubmed-3762023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37620232013-09-11 Sirenomelia Apus: A Rare Deformity Kshirsagar, Vinayak Y. Ahmed, Minhajuddin Colaco, Sylvia M. J Clin Neonatol Case Report Sirenomelia also known as the mermaid syndrome, is a rare congenital malformation of uncertain etiology. It is characterized by fusion of the lower limbs and commonly associated with severe urogenital and gastrointestinal malformations. There are approximately 300 cases reported in the literature, 15% of which are associated with twinning, most often monozygotic. The syndrome of caudal regression is thought to be the result of injury to the caudal mesoderm early in gestation. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3762023/ /pubmed/24027712 http://dx.doi.org/10.4103/2249-4847.101699 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 Kshirsagar, Vinayak Y. Ahmed, Minhajuddin Colaco, Sylvia M. Sirenomelia Apus: A Rare Deformity |
title | Sirenomelia Apus: A Rare Deformity |
title_full | Sirenomelia Apus: A Rare Deformity |
title_fullStr | Sirenomelia Apus: A Rare Deformity |
title_full_unstemmed | Sirenomelia Apus: A Rare Deformity |
title_short | Sirenomelia Apus: A Rare Deformity |
title_sort | sirenomelia apus: a rare deformity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762023/ https://www.ncbi.nlm.nih.gov/pubmed/24027712 http://dx.doi.org/10.4103/2249-4847.101699 |
work_keys_str_mv | AT kshirsagarvinayaky sirenomeliaapusararedeformity AT ahmedminhajuddin sirenomeliaapusararedeformity AT colacosylviam sirenomeliaapusararedeformity |