- Dentinogenesis imperfecta type II: A case report with 17 years of follow-up
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Gama FJ, Corrêa IS, Valerio CS, Ferreira E, Manzi FR
- KMID: 2389894
- Imaging Sci Dent.
- 2017 Jun;47(2):129-133.
- doi: 10.5624/isd.2017.47.2.129
Dentinogenesis imperfecta is a dominant autosomal hereditary disorder of dentin formation that affects the deciduous and permanent teeth. Its etiology is characterized by inadequate cell differentiation during odontogenesis. The clinical... -
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