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Dentinogenesis imperfecta

Author:

Mahesh C.M., Bobby Joseph Babu, Balamohan Shetty and Harish Koushik

Subject Area:

Health Sciences

Abstract:

Dentinogenesis imperfecta is one of the most common hereditary disorders of dentin formation. It follows an autosomal pattern of transmission, affecting both the formation and mineralization of dentin. Either or both primary and permanent dentition is affected by it. This paper describes a case of Dentinogenesis imperfecta which reported for orthodontic treatment.

PDF file:

20095.pdf

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