Guitelman IC, Fridman DE, Moya MA

Language: Spanish
References: 15
Page: 136-145
PDF size: 1143.87 Kb.

ABSTRACT

Dentinogenesis Imperfecta is a genetically determinated dental abnormality, characterized clinically by opalescent and translucent appearance of the dentin. Clinical management and a 12 years follow up are reported, in a 3 years old patient with Dentinogenesis Imperfecta type I associated with Osteogenesis Imperfecta type IB. The earlier diagnosis and the opportune and multidisciplinary treatment, led to improve the prognosis.

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