Orthodontic Treatment of a Patient with Dentin Dysplasia Type I and Bilateral Maxillary Canine Impaction: Case Presentation and a Family-Based Genetic Analysis

Dentin dysplasia is a rare hereditary disorder, transmitted by autosomal dominant mode, affecting both dentin and pulp. In Type I crown morphology is normal, but root dentin organization loss leads to shorter roots. Mutations in the <i>SSUH2</i>, <i>VPS4B</i> and <i>SMO...

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Bibliographic Details
Main Authors: Alexandros Papagiannis, Galinos Fanourakis, Anastasia Mitsea, Kety Karayianni, Heleni Vastardis, Iosif Sifakakis
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Children
Subjects:
Online Access:https://www.mdpi.com/2227-9067/8/6/519