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Dentin dysplasia type I – A rare entity
Dentin dysplasia is a rare disturbance of dentin formation characterized by normal enamel but atypical dentin formation with abnormal pupal morphology. The teeth appear clinically normal in morphologic appearance and color. The teeth characteristically exhibit extreme mobility and are commonly exfol...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451656/ https://www.ncbi.nlm.nih.gov/pubmed/26097326 http://dx.doi.org/10.4103/0973-029X.157220 |
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author | Malik, Sangeeta Gupta, Swati Wadhwan, Vijay Suhasini, GP |
author_facet | Malik, Sangeeta Gupta, Swati Wadhwan, Vijay Suhasini, GP |
author_sort | Malik, Sangeeta |
collection | PubMed |
description | Dentin dysplasia is a rare disturbance of dentin formation characterized by normal enamel but atypical dentin formation with abnormal pupal morphology. The teeth appear clinically normal in morphologic appearance and color. The teeth characteristically exhibit extreme mobility and are commonly exfoliated prematurely. Radiograph shows obliteration of all pulp chambers, short, blunted and malformed or absent roots with periapical radiolucencies involving apparently intact tooth. This case is reported here because of its rarity along with the description of various clinical, radiological and histological features. |
format | Online Article Text |
id | pubmed-4451656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44516562015-06-19 Dentin dysplasia type I – A rare entity Malik, Sangeeta Gupta, Swati Wadhwan, Vijay Suhasini, GP J Oral Maxillofac Pathol Case Report Dentin dysplasia is a rare disturbance of dentin formation characterized by normal enamel but atypical dentin formation with abnormal pupal morphology. The teeth appear clinically normal in morphologic appearance and color. The teeth characteristically exhibit extreme mobility and are commonly exfoliated prematurely. Radiograph shows obliteration of all pulp chambers, short, blunted and malformed or absent roots with periapical radiolucencies involving apparently intact tooth. This case is reported here because of its rarity along with the description of various clinical, radiological and histological features. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4451656/ /pubmed/26097326 http://dx.doi.org/10.4103/0973-029X.157220 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 Malik, Sangeeta Gupta, Swati Wadhwan, Vijay Suhasini, GP Dentin dysplasia type I – A rare entity |
title | Dentin dysplasia type I – A rare entity |
title_full | Dentin dysplasia type I – A rare entity |
title_fullStr | Dentin dysplasia type I – A rare entity |
title_full_unstemmed | Dentin dysplasia type I – A rare entity |
title_short | Dentin dysplasia type I – A rare entity |
title_sort | dentin dysplasia type i – a rare entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451656/ https://www.ncbi.nlm.nih.gov/pubmed/26097326 http://dx.doi.org/10.4103/0973-029X.157220 |
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