Dentinogenesis Imperfecta Type I and II: A Case Series Highlighting Clinical and Radiographic Insights
Dentinogenesis imperfecta (DI) is a rare hereditary disorder affecting the dentin structure of both primary and permanent teeth, characterized by discoloration, structural fragility, and distinctive radiographic features. It is classified into three types, with Type I associated with osteogenesis im...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wolters Kluwer Medknow Publications
2025-10-01
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| Seri Bilgileri: | Indian Journal of Dental Sciences |
| Konular: | |
| Online Erişim: | https://journals.lww.com/10.4103/ijds.ijds_84_25 |
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