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Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos

Vieira, Heloisa Aparecida Orsini; Freitas, Aldevina Campos de; Fernandes, Regina Maura; Longo, Daniele Lucca; Silva, Raquel Assed Bezerra da

Dentinogenesis imperfecta (DI) is a hereditary developmental disorder of dentin formation that can occur associated with osteogenesis imperfecta (type I), isolated (type II), or in a specific isolated resident group of Brandywine, in southern Maryland (type III). This work aims at reporting a clinical case of DI type II in childhood with a 34-year follow up. The child at issue was taken to the dental health ser...

Date: 2020   |   Origin: Oasisbr







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