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Conjoined legs: Sirenomelia or caudal regression syndrome?
Presence of single umbilical persistent vitelline artery distinguishes sirenomelia from caudal regression syndrome. We report a case of a12-year-old boy who had bilateral umbilical arteries presented with fusion of both legs in the lower one third of leg. Both feet were rudimentary. The right foot h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745698/ https://www.ncbi.nlm.nih.gov/pubmed/23960288 http://dx.doi.org/10.4103/0019-5413.114936 |
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author | Das, Sakti Prasad Ojha, Niranjan Ganesh, G Shankar Mohanty, Ram Narayan |
author_facet | Das, Sakti Prasad Ojha, Niranjan Ganesh, G Shankar Mohanty, Ram Narayan |
author_sort | Das, Sakti Prasad |
collection | PubMed |
description | Presence of single umbilical persistent vitelline artery distinguishes sirenomelia from caudal regression syndrome. We report a case of a12-year-old boy who had bilateral umbilical arteries presented with fusion of both legs in the lower one third of leg. Both feet were rudimentary. The right foot had a valgus rocker-bottom deformity. All toes were present but rudimentary. The left foot showed absence of all toes. Physical examination showed left tibia vara. The chest evaluation in sitting revealed pigeon chest and elevated right shoulder. Posterior examination of the trunk showed thoracic scoliosis with convexity to right. The patient was operated and at 1 year followup the boy had two separate legs with a good aesthetic and functional results. |
format | Online Article Text |
id | pubmed-3745698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37456982013-08-19 Conjoined legs: Sirenomelia or caudal regression syndrome? Das, Sakti Prasad Ojha, Niranjan Ganesh, G Shankar Mohanty, Ram Narayan Indian J Orthop Case Report Presence of single umbilical persistent vitelline artery distinguishes sirenomelia from caudal regression syndrome. We report a case of a12-year-old boy who had bilateral umbilical arteries presented with fusion of both legs in the lower one third of leg. Both feet were rudimentary. The right foot had a valgus rocker-bottom deformity. All toes were present but rudimentary. The left foot showed absence of all toes. Physical examination showed left tibia vara. The chest evaluation in sitting revealed pigeon chest and elevated right shoulder. Posterior examination of the trunk showed thoracic scoliosis with convexity to right. The patient was operated and at 1 year followup the boy had two separate legs with a good aesthetic and functional results. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3745698/ /pubmed/23960288 http://dx.doi.org/10.4103/0019-5413.114936 Text en Copyright: © Indian Journal of Orthopaedics 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 Das, Sakti Prasad Ojha, Niranjan Ganesh, G Shankar Mohanty, Ram Narayan Conjoined legs: Sirenomelia or caudal regression syndrome? |
title | Conjoined legs: Sirenomelia or caudal regression syndrome? |
title_full | Conjoined legs: Sirenomelia or caudal regression syndrome? |
title_fullStr | Conjoined legs: Sirenomelia or caudal regression syndrome? |
title_full_unstemmed | Conjoined legs: Sirenomelia or caudal regression syndrome? |
title_short | Conjoined legs: Sirenomelia or caudal regression syndrome? |
title_sort | conjoined legs: sirenomelia or caudal regression syndrome? |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745698/ https://www.ncbi.nlm.nih.gov/pubmed/23960288 http://dx.doi.org/10.4103/0019-5413.114936 |
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