Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report
Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal dominant mutation in dentin sialophosphoprotein gene. Defective dentin development results in discolored teeth that are prone to wear and fracture. Early diagnosis and proper treatment are necessary to achieve better...
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| Main Authors: | , , |
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| Format: | Book |
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Tehran University of Medical Sciences,
2016-10-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |