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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Detalles Bibliográficos
Autores principales: Gama, Francisco José Reis, Corrêa, Isabella Sousa, Valerio, Claudia Scigliano, Ferreira, Emanuelle de Fátima, Manzi, Flávio Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Academy of Oral and Maxillofacial Radiology 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489669/
https://www.ncbi.nlm.nih.gov/pubmed/28680850
http://dx.doi.org/10.5624/isd.2017.47.2.129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489669/
https://www.ncbi.nlm.nih.gov/pubmed/28680850
http://dx.doi.org/10.5624/isd.2017.47.2.129

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