Prosthetic treatment in dentinogenesis imperfecta type II: a case report

• Váldodahkkit: Sedat Güven (Dahkki), Fatih Demirci (Dahkki), Abdulsamet Tanik (Dahkki), Mahmut Koparal (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: Gazi University, 2016-05-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

INTRODUCTION: Dentinogenesis imperfecta (DI) or hereditary opalescent dentin is an autosomal dominant disorder affecting both primary and permanent dentition. Early diagnosis and treatment of DI is important for normal facial growth and esthetic continuity by preserving occlusion and tooth structure...