Ellis–Van Creveld syndrome in siblings: A rare case report

Ellis–Van Creveld syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder presenting several skeletal manifestations and congenital heart malformations. Ellis–Van Creveld syndrome comprises of a tetrad of clinical manifestations of chondrodysplasia, polydactyly, ectodermal dys...

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Autores principales: Gokulraj, Sabitha, Mohan, N., Raj, J. Babususai, Ahamed, S. Yasmeen, Arokiaraj, C. J. Stephen, Subbulakshmi, A. Cicilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074027/
https://www.ncbi.nlm.nih.gov/pubmed/27829775
http://dx.doi.org/10.4103/0975-7406.191954
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author Gokulraj, Sabitha
Mohan, N.
Raj, J. Babususai
Ahamed, S. Yasmeen
Arokiaraj, C. J. Stephen
Subbulakshmi, A. Cicilia
author_facet Gokulraj, Sabitha
Mohan, N.
Raj, J. Babususai
Ahamed, S. Yasmeen
Arokiaraj, C. J. Stephen
Subbulakshmi, A. Cicilia
author_sort Gokulraj, Sabitha
collection PubMed
description Ellis–Van Creveld syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder presenting several skeletal manifestations and congenital heart malformations. Ellis–Van Creveld syndrome comprises of a tetrad of clinical manifestations of chondrodysplasia, polydactyly, ectodermal dysplasia, and cardiac defects. Here, we are presenting a very rare case of Ellis–Van Creveld syndrome in siblings.
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spelling pubmed-50740272016-11-09 Ellis–Van Creveld syndrome in siblings: A rare case report Gokulraj, Sabitha Mohan, N. Raj, J. Babususai Ahamed, S. Yasmeen Arokiaraj, C. J. Stephen Subbulakshmi, A. Cicilia J Pharm Bioallied Sci Case Report Ellis–Van Creveld syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder presenting several skeletal manifestations and congenital heart malformations. Ellis–Van Creveld syndrome comprises of a tetrad of clinical manifestations of chondrodysplasia, polydactyly, ectodermal dysplasia, and cardiac defects. Here, we are presenting a very rare case of Ellis–Van Creveld syndrome in siblings. Medknow Publications & Media Pvt Ltd 2016-10 /pmc/articles/PMC5074027/ /pubmed/27829775 http://dx.doi.org/10.4103/0975-7406.191954 Text en Copyright: © Journal of Pharmacy And Bioallied Sciences 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Gokulraj, Sabitha
Mohan, N.
Raj, J. Babususai
Ahamed, S. Yasmeen
Arokiaraj, C. J. Stephen
Subbulakshmi, A. Cicilia
Ellis–Van Creveld syndrome in siblings: A rare case report
title Ellis–Van Creveld syndrome in siblings: A rare case report
title_full Ellis–Van Creveld syndrome in siblings: A rare case report
title_fullStr Ellis–Van Creveld syndrome in siblings: A rare case report
title_full_unstemmed Ellis–Van Creveld syndrome in siblings: A rare case report
title_short Ellis–Van Creveld syndrome in siblings: A rare case report
title_sort ellis–van creveld syndrome in siblings: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074027/
https://www.ncbi.nlm.nih.gov/pubmed/27829775
http://dx.doi.org/10.4103/0975-7406.191954
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