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Chondroectodermal Dysplasia: A Rare Syndrome

Chondroectodermal dysplasia (Ellis-Van Creveld syndrome) is a rare autosomal recessive congenital abnormality. This syndrome is characterized by a spectrum of clinical findings, among which chondrodystrophy, polydactyly, ectodermal dysplasia, and congenital cardiac anomalies are the most common. It...

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Autores principales: Tahririan, Dana, Eshghi, Alireza, Givehchian, Pirooz, Tahririan, Mohammad Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290765/
https://www.ncbi.nlm.nih.gov/pubmed/25628672
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author Tahririan, Dana
Eshghi, Alireza
Givehchian, Pirooz
Tahririan, Mohammad Ali
author_facet Tahririan, Dana
Eshghi, Alireza
Givehchian, Pirooz
Tahririan, Mohammad Ali
author_sort Tahririan, Dana
collection PubMed
description Chondroectodermal dysplasia (Ellis-Van Creveld syndrome) is a rare autosomal recessive congenital abnormality. This syndrome is characterized by a spectrum of clinical findings, among which chondrodystrophy, polydactyly, ectodermal dysplasia, and congenital cardiac anomalies are the most common. It is imperative to not overlook the cardiac complications in patients with this syndrome during dental procedures. The case presented here, although quite rare, was detected under normal conditions and can be alarming for dental care providers. Clinical reports outline the classical and unusual oral and dental manifestations, which help health care providers diagnose chondroectodermal dysplasia, and refer patients with this syndrome to appropriate health care professionals to receive treatment to prevent further cardiac complications and bone deformities.
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spelling pubmed-42907652015-01-27 Chondroectodermal Dysplasia: A Rare Syndrome Tahririan, Dana Eshghi, Alireza Givehchian, Pirooz Tahririan, Mohammad Ali J Dent (Tehran) Case Report Chondroectodermal dysplasia (Ellis-Van Creveld syndrome) is a rare autosomal recessive congenital abnormality. This syndrome is characterized by a spectrum of clinical findings, among which chondrodystrophy, polydactyly, ectodermal dysplasia, and congenital cardiac anomalies are the most common. It is imperative to not overlook the cardiac complications in patients with this syndrome during dental procedures. The case presented here, although quite rare, was detected under normal conditions and can be alarming for dental care providers. Clinical reports outline the classical and unusual oral and dental manifestations, which help health care providers diagnose chondroectodermal dysplasia, and refer patients with this syndrome to appropriate health care professionals to receive treatment to prevent further cardiac complications and bone deformities. Tehran University of Medical Sciences 2014-05 2014-05-31 /pmc/articles/PMC4290765/ /pubmed/25628672 Text en Copyright © Dental Research Center, Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Case Report
Tahririan, Dana
Eshghi, Alireza
Givehchian, Pirooz
Tahririan, Mohammad Ali
Chondroectodermal Dysplasia: A Rare Syndrome
title Chondroectodermal Dysplasia: A Rare Syndrome
title_full Chondroectodermal Dysplasia: A Rare Syndrome
title_fullStr Chondroectodermal Dysplasia: A Rare Syndrome
title_full_unstemmed Chondroectodermal Dysplasia: A Rare Syndrome
title_short Chondroectodermal Dysplasia: A Rare Syndrome
title_sort chondroectodermal dysplasia: a rare syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290765/
https://www.ncbi.nlm.nih.gov/pubmed/25628672
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