VOHRA PRIYANKA

Dentinogenesis Imperfecta Type I Associated with Osteogenesis Imperfecta: Clinical, Radiographic, and Histopathological Findings

Background: Dentinogenesis imperfecta (DI) is an autosomal dominant hereditary developmental defect of dentin that affects both primary and permanent teeth. DI Type I is linked with OI (osteogenesis imperfecta), a generalized connective tissue disorder characterized by increased...

Dentinogenesis Imperfecta Type I Associated with Osteogenesis Imperfecta: Clinical, Radiographic, and Histopathological Findings

Background: Dentinogenesis imperfecta (DI) is an autosomal dominant hereditary developmental defect of dentin that affects both primary and permanent teeth. DI Type I is linked with OI (osteogenesis imperfecta), a generalized connective tissue disorder characterized by increased...