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Orofacial manifestations of achondroplasia
Achondroplasia (Online Mendelian Inheritance in Man [OMIM] 100800), is considered as a form of skeletal dysplasia dwarfism that manifests with stunted stature and disproportionate limb shortening. Achondroplasia is of special interest in the field of dentistry because of its characteristic craniofac...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Leibniz Research Centre for Working Environment and Human Factors
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897656/ https://www.ncbi.nlm.nih.gov/pubmed/27298609 |
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author | Rohilla, Smriti Kaushik, Atul Vinod, V.C. Tanwar, Renu Kumar, Munish |
author_facet | Rohilla, Smriti Kaushik, Atul Vinod, V.C. Tanwar, Renu Kumar, Munish |
author_sort | Rohilla, Smriti |
collection | PubMed |
description | Achondroplasia (Online Mendelian Inheritance in Man [OMIM] 100800), is considered as a form of skeletal dysplasia dwarfism that manifests with stunted stature and disproportionate limb shortening. Achondroplasia is of special interest in the field of dentistry because of its characteristic craniofacial features which include relative macrocephaly, depressed nasal bridge and maxillary hypoplasia. Presence of large head, implanted shunt, airway obstruction and difficulty in head control requires special precautions during dental management. The current case report highlights the orofacial manifestations of Achondroplasia in a young pediatric patient, along with the multidisciplinary treatment (including the dental treatment) done for the patient which also might help the general practitioners in better understanding of the condition. |
format | Online Article Text |
id | pubmed-4897656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Leibniz Research Centre for Working Environment and Human Factors |
record_format | MEDLINE/PubMed |
spelling | pubmed-48976562016-06-13 Orofacial manifestations of achondroplasia Rohilla, Smriti Kaushik, Atul Vinod, V.C. Tanwar, Renu Kumar, Munish EXCLI J Case Report Achondroplasia (Online Mendelian Inheritance in Man [OMIM] 100800), is considered as a form of skeletal dysplasia dwarfism that manifests with stunted stature and disproportionate limb shortening. Achondroplasia is of special interest in the field of dentistry because of its characteristic craniofacial features which include relative macrocephaly, depressed nasal bridge and maxillary hypoplasia. Presence of large head, implanted shunt, airway obstruction and difficulty in head control requires special precautions during dental management. The current case report highlights the orofacial manifestations of Achondroplasia in a young pediatric patient, along with the multidisciplinary treatment (including the dental treatment) done for the patient which also might help the general practitioners in better understanding of the condition. Leibniz Research Centre for Working Environment and Human Factors 2012-08-27 /pmc/articles/PMC4897656/ /pubmed/27298609 Text en Copyright © 2012 Rohilla et al. http://www.excli.de/documents/assignment_of_rights.pdf This is an Open Access article distributed under the following Assignment of Rights http://www.excli.de/documents/assignment_of_rights.pdf. You are free to copy, distribute and transmit the work, provided the original author and source are credited. |
spellingShingle | Case Report Rohilla, Smriti Kaushik, Atul Vinod, V.C. Tanwar, Renu Kumar, Munish Orofacial manifestations of achondroplasia |
title | Orofacial manifestations of achondroplasia |
title_full | Orofacial manifestations of achondroplasia |
title_fullStr | Orofacial manifestations of achondroplasia |
title_full_unstemmed | Orofacial manifestations of achondroplasia |
title_short | Orofacial manifestations of achondroplasia |
title_sort | orofacial manifestations of achondroplasia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897656/ https://www.ncbi.nlm.nih.gov/pubmed/27298609 |
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