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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Detalles Bibliográficos
Autores principales: Akhlaghi, Najmeh, Eshghi, Ali-Reza, Mohamadpour, Mehrnaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139931/
https://www.ncbi.nlm.nih.gov/pubmed/27928242

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139931/
https://www.ncbi.nlm.nih.gov/pubmed/27928242

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