| Literature DB >> 29895546 |
Ahmed Alhilou1, Hannah P Beddis1, Alan J Mighell2, Kathryn Durey1.
Abstract
Dentin dysplasia(DD) is a rare autosomal dominant disorder associated with disturbance of the dentin. While the crowns appear clinically normal, on radiography, the pulp spaces appear partially or completely obliterated, with short blunted roots, and multiple periapical radiolucencies affecting the apparently sound teeth. Clinical signs include spontaneous abscess formation or increased tooth mobility which can lead to exfoliation. DD can therefore have a significant impact on the patient's dentition, and treatment is often challenging. Shields' classification of dentin disorders has been recently criticised for failing to consider differential variations and expressions of these disorders. This paper describes a case of a 23-year-old woman with previously undiagnosed DD, who presented with clinical and histological features belonging to several of these diseases, thus highlighting the potential diagnostic challenges faced with Shields' classification. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: dentistry and oral medicine; genetics
Mesh:
Year: 2018 PMID: 29895546 PMCID: PMC6011466 DOI: 10.1136/bcr-2017-223942
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X