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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| Автори: | , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Wolters Kluwer Medknow Publications
2025-10-01
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| Серія: | Indian Journal of Dental Sciences |
| Предмети: | |
| Онлайн доступ: | https://journals.lww.com/10.4103/ijds.ijds_84_25 |
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