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...

全面介绍

Saved in:
书目详细资料
Main Authors: Najmeh Akhlaghi (Author), Ali-Reza Eshghi (Author), Mehrnaz Mohamadpour (Author)
格式: 图书
出版: Tehran University of Medical Sciences, 2016-10-01T00:00:00Z.
主题:
在线阅读:Connect to this object online.
标签: 添加标签
没有标签, 成为第一个标记此记录!

因特网

Connect to this object online.

3rd Floor Main Library

持有资料详情 3rd Floor Main Library
索引号: A1234.567
复印件 1 可用