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Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis

Dentin dysplasia is a rare inherited autosomal dominant disorder characterized by rootless teeth. We hereby report a case of dentin dysplasia type 1b with typical radiographic findings: short and blunt roots, pulpal obliteration, horizontal/crescent shaped radiolucencies in pulp chambers, and multip...

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Autores principales: Suman, S. Venkata, Jayam, Raviraj, Kumar, B. Vijay, Dirasantchu, Suresh, Kumar, K. Venkata Suneel, Sk, Sameeulla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866844/
https://www.ncbi.nlm.nih.gov/pubmed/24367729
http://dx.doi.org/10.1155/2013/902861
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author Suman, S. Venkata
Jayam, Raviraj
Kumar, B. Vijay
Dirasantchu, Suresh
Kumar, K. Venkata Suneel
Sk, Sameeulla
author_facet Suman, S. Venkata
Jayam, Raviraj
Kumar, B. Vijay
Dirasantchu, Suresh
Kumar, K. Venkata Suneel
Sk, Sameeulla
author_sort Suman, S. Venkata
collection PubMed
description Dentin dysplasia is a rare inherited autosomal dominant disorder characterized by rootless teeth. We hereby report a case of dentin dysplasia type 1b with typical radiographic findings: short and blunt roots, pulpal obliteration, horizontal/crescent shaped radiolucencies in pulp chambers, and multiple periapical radiolucencies. However, the present case did not show the autosomal dominant pattern of inheritance and the patient also exhibited concurrent dental fluorosis, transposition of 13 and 14, and multiple cusps in maxillary first molars. Moreover, on careful review of previously documented cases of radiographs of dentin dysplasia, the horizontal/crescent shaped radiolucencies in pulp chambers are a rare finding, which is characteristically seen in the present case.
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spelling pubmed-38668442013-12-23 Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis Suman, S. Venkata Jayam, Raviraj Kumar, B. Vijay Dirasantchu, Suresh Kumar, K. Venkata Suneel Sk, Sameeulla Case Rep Dent Case Report Dentin dysplasia is a rare inherited autosomal dominant disorder characterized by rootless teeth. We hereby report a case of dentin dysplasia type 1b with typical radiographic findings: short and blunt roots, pulpal obliteration, horizontal/crescent shaped radiolucencies in pulp chambers, and multiple periapical radiolucencies. However, the present case did not show the autosomal dominant pattern of inheritance and the patient also exhibited concurrent dental fluorosis, transposition of 13 and 14, and multiple cusps in maxillary first molars. Moreover, on careful review of previously documented cases of radiographs of dentin dysplasia, the horizontal/crescent shaped radiolucencies in pulp chambers are a rare finding, which is characteristically seen in the present case. Hindawi Publishing Corporation 2013 2013-12-03 /pmc/articles/PMC3866844/ /pubmed/24367729 http://dx.doi.org/10.1155/2013/902861 Text en Copyright © 2013 S. Venkata Suman et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Suman, S. Venkata
Jayam, Raviraj
Kumar, B. Vijay
Dirasantchu, Suresh
Kumar, K. Venkata Suneel
Sk, Sameeulla
Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis
title Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis
title_full Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis
title_fullStr Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis
title_full_unstemmed Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis
title_short Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis
title_sort typical radiographic findings of dentin dysplasia type 1b with dental fluorosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866844/
https://www.ncbi.nlm.nih.gov/pubmed/24367729
http://dx.doi.org/10.1155/2013/902861
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