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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....
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/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. |
format | Online Article Text |
id | pubmed-3687170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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