Dentinogenesis imperfecta type II: A case report with 17 years of follow-up

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 characteristics of dentinogenesis imperfecta are discolored te...

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Bibliographic Details
Published in:Imaging Sci Dent
Main Authors: Gama, Francisco José Reis, Corrêa, Isabella Sousa, Valerio, Claudia Scigliano, Ferreira, Emanuelle de Fátima, Manzi, Flávio Ricardo
Format: Artigo
Language:Inglês
Published: Korean Academy of Oral and Maxillofacial Radiology 2017
Subjects:
Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5489669/
https://ncbi.nlm.nih.gov/pubmed/28680850
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5624/isd.2017.47.2.129
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