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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...

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Autores principales: Malik, Sangeeta, Gupta, Swati, Wadhwan, Vijay, Suhasini, GP
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
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.
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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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AT wadhwanvijay dentindysplasiatypeiarareentity
AT suhasinigp dentindysplasiatypeiarareentity