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A Case of Dentinogenesis Imperfecta Treated with Submerged Root Technique
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 aff...
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| 出版年: | J Clin Diagn Res |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
JCDR Research and Publications (P) Limited
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4606354/ https://ncbi.nlm.nih.gov/pubmed/26501025 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2015/13340.6471 |
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