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Dentin dysplasia type I.

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.
AuthorsAarti Singh, Sangesh Gupta, Monal Bhaurao Yuwanati, Shubhangi Mhaske
JournalBMJ case reports (BMJ Case Rep) Vol. 2013 (Jun 27 2013) ISSN: 1757-790X [Electronic] England
PMID23814198 (Publication Type: Case Reports, Journal Article)
Topics
  • Adolescent
  • Child
  • Dentin Dysplasia (diagnosis)
  • Female
  • Humans
  • Male

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