Abstract
Study of enamel and dentin in primary teeth with dentinogenesis imperfecta type I: A case report
Highlights
Dentinogenesis imperfecta (DI) is a rare genetic disease affecting the development of dentin, and it is clinically characterized by tooth discoloration and early enamel loss
DI-type I may be seen in conjunction with osteogenesis imperfecta (OI), which is a disease characterized by fragile bones resulting from genetic mutations that impair collagen synthesis [2,7]
After Raman analysis, each specimen was coated with gold and the microstructure of enamel and dentin was examined using scanning electron microscopy (SEM) (S-3500, Hitachi Ltd., Tokyo, Japan) (Figure 4)
Summary
Study of enamel and dentin in primary teeth with dentinogenesis imperfecta type I: A case report.
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