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Ellis-van Creveld syndrome: A rare clinical entity

Ellis-van Creveld (EVC) syndrome is a genetic disorder with autosomal recessive transmission, which may clinically present as small stature, short limbs, fine sparse hair, hypoplastic fingernails, multiple musculofibrous frenula, conical teeth, hypoplasia of the enamel, hypodontia, and malocclusion....

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Detalles Bibliográficos
Autores principales: Kamal, Reet, Dahiya, Parveen, Kaur, Simerpreet, Bhardwaj, Rohit, Chaudhary, Karun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687170/
https://www.ncbi.nlm.nih.gov/pubmed/23798848
http://dx.doi.org/10.4103/0973-029X.110716
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author Kamal, Reet
Dahiya, Parveen
Kaur, Simerpreet
Bhardwaj, Rohit
Chaudhary, Karun
author_facet Kamal, Reet
Dahiya, Parveen
Kaur, Simerpreet
Bhardwaj, Rohit
Chaudhary, Karun
author_sort Kamal, Reet
collection PubMed
description Ellis-van Creveld (EVC) syndrome is a genetic disorder with autosomal recessive transmission, which may clinically present as small stature, short limbs, fine sparse hair, hypoplastic fingernails, multiple musculofibrous frenula, conical teeth, hypoplasia of the enamel, hypodontia, and malocclusion. Heart defects, especially abnormalities of atrial septation, have been found in about 60% of cases. The mutation in EVC and EVC2 gene is responsible for this syndrome. The presence of multiple orodental findings makes this syndrome important for dentists. The aim of this article is to present a rare case of EVC syndrome in a 10-year-old girl along with the review of literature.
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spelling pubmed-36871702013-06-24 Ellis-van Creveld syndrome: A rare clinical entity Kamal, Reet Dahiya, Parveen Kaur, Simerpreet Bhardwaj, Rohit Chaudhary, Karun J Oral Maxillofac Pathol Case Report Ellis-van Creveld (EVC) syndrome is a genetic disorder with autosomal recessive transmission, which may clinically present as small stature, short limbs, fine sparse hair, hypoplastic fingernails, multiple musculofibrous frenula, conical teeth, hypoplasia of the enamel, hypodontia, and malocclusion. Heart defects, especially abnormalities of atrial septation, have been found in about 60% of cases. The mutation in EVC and EVC2 gene is responsible for this syndrome. The presence of multiple orodental findings makes this syndrome important for dentists. The aim of this article is to present a rare case of EVC syndrome in a 10-year-old girl along with the review of literature. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3687170/ /pubmed/23798848 http://dx.doi.org/10.4103/0973-029X.110716 Text en Copyright: © Journal of Oral and Maxillofacial Pathology 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
Kamal, Reet
Dahiya, Parveen
Kaur, Simerpreet
Bhardwaj, Rohit
Chaudhary, Karun
Ellis-van Creveld syndrome: A rare clinical entity
title Ellis-van Creveld syndrome: A rare clinical entity
title_full Ellis-van Creveld syndrome: A rare clinical entity
title_fullStr Ellis-van Creveld syndrome: A rare clinical entity
title_full_unstemmed Ellis-van Creveld syndrome: A rare clinical entity
title_short Ellis-van Creveld syndrome: A rare clinical entity
title_sort ellis-van creveld syndrome: a rare clinical entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687170/
https://www.ncbi.nlm.nih.gov/pubmed/23798848
http://dx.doi.org/10.4103/0973-029X.110716
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