Dentinogenesis imperfecta is a hereditary and developmental disturbance of the dentin which may be isolated or may occur in association with a number of syndromes. It is divided into three main types: type 1, type 2 and type 3. Type 1 Dentinogenesis imperfecta is always associated with osteogenesis imperfecta while type 2 and type 3 arises in isolated forms.

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Video(diagrams+editing) & Voiceover:
Dr.Maryam Kazman

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