| Literature DB >> 23814198 |
Aarti Singh1, Sangesh Gupta, Monal Bhaurao Yuwanati, Shubhangi Mhaske.
Abstract
Dentin dysplasia type I is a rare hereditary disturbance of dentin formation characterised clinically by nearly normal appearing crowns and hypermobility of teeth that affects one in every 100,000 individuals and manifests in both primary and permanent dentitions. Radiographic analysis shows obliteration of all pulp chambers, short, blunted, and malformed roots, and periapical radiolucencies of non-carious teeth. This paper presents three cases demonstrating classic features of type I dentin dysplasia.Entities:
Mesh:
Year: 2013 PMID: 23814198 PMCID: PMC3702896 DOI: 10.1136/bcr-2013-009403
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X