| Literature DB >> 26501025 |
Ginjupally Uday1, Bhanu Chandar2, J Srilakshmi3, Tanya Khaitan4, B Balaji Babu5.
Abstract
Dentinogenesis imperfecta (DGI), an autosomal dominant trait, is one of the most common hereditary disorders affecting both the formation and mineralization of dentin. Either or both primary and permanent dentition is affected by it. Here, we present a case report of a 13-year-old female patient affected with DGI who had undergone prosthetic rehabilitation with submerged root technique.Entities:
Keywords: Defective dentin; Dentition; Hereditary opalescent dentin
Year: 2015 PMID： 26501025 PMCID： PMC4606354 DOI： 10.7860/JCDR/2015/13340.6471
Source DB: PubMed Journal: J Clin Diagn Res ISSN： 0973-709X