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Sirenomelia: The mermaid syndrome: Report of two cases

Sirenomelia (mermaid syndrome) is a rare congenital fetal anomaly with characteristic feature of complete or partial fusion of lower limbs. Although, this syndrome is incompatible with life due to the association of several congenital visceral abnormalities; however, there are few reports of survivi...

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Detalles Bibliográficos
Autores principales: Samal, Sunil Kumar, Rathod, Setu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367057/
https://www.ncbi.nlm.nih.gov/pubmed/25810681
http://dx.doi.org/10.4103/0976-9668.149227
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author Samal, Sunil Kumar
Rathod, Setu
author_facet Samal, Sunil Kumar
Rathod, Setu
author_sort Samal, Sunil Kumar
collection PubMed
description Sirenomelia (mermaid syndrome) is a rare congenital fetal anomaly with characteristic feature of complete or partial fusion of lower limbs. Although, this syndrome is incompatible with life due to the association of several congenital visceral abnormalities; however, there are few reports of surviving infants. Our first case was a live born, normally delivered at term by a 27-year-old third gravida of lower socioeconomic status with history of tobacco use. Examination of the baby revealed caudal dysgenesis having fusion of lower limbs, single leg with 1 foot and 5 toes. There was no identifiable external genitalia and anus. The second case was a 34 week, 1.6 kg preterm infant of unidentified sex born to a 28-year-old primigravida mother with overt diabetes mellitus. Incidentally, both the infants died few hours after birth and we report these cases due to their rarity and term live birth.
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spelling pubmed-43670572015-03-25 Sirenomelia: The mermaid syndrome: Report of two cases Samal, Sunil Kumar Rathod, Setu J Nat Sci Biol Med Case Report Sirenomelia (mermaid syndrome) is a rare congenital fetal anomaly with characteristic feature of complete or partial fusion of lower limbs. Although, this syndrome is incompatible with life due to the association of several congenital visceral abnormalities; however, there are few reports of surviving infants. Our first case was a live born, normally delivered at term by a 27-year-old third gravida of lower socioeconomic status with history of tobacco use. Examination of the baby revealed caudal dysgenesis having fusion of lower limbs, single leg with 1 foot and 5 toes. There was no identifiable external genitalia and anus. The second case was a 34 week, 1.6 kg preterm infant of unidentified sex born to a 28-year-old primigravida mother with overt diabetes mellitus. Incidentally, both the infants died few hours after birth and we report these cases due to their rarity and term live birth. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4367057/ /pubmed/25810681 http://dx.doi.org/10.4103/0976-9668.149227 Text en Copyright: © Journal of Natural Science, Biology and Medicine 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
Samal, Sunil Kumar
Rathod, Setu
Sirenomelia: The mermaid syndrome: Report of two cases
title Sirenomelia: The mermaid syndrome: Report of two cases
title_full Sirenomelia: The mermaid syndrome: Report of two cases
title_fullStr Sirenomelia: The mermaid syndrome: Report of two cases
title_full_unstemmed Sirenomelia: The mermaid syndrome: Report of two cases
title_short Sirenomelia: The mermaid syndrome: Report of two cases
title_sort sirenomelia: the mermaid syndrome: report of two cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367057/
https://www.ncbi.nlm.nih.gov/pubmed/25810681
http://dx.doi.org/10.4103/0976-9668.149227
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