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

• Egile Nagusiak: Alexandros Papagiannis (Egilea), Galinos Fanourakis (Egilea), Anastasia Mitsea (Egilea), Kety Karayianni (Egilea), Heleni Vastardis (Egilea), Iosif Sifakakis (Egilea)
• Formatua: Liburua
• Argitaratua: MDPI AG, 2021-06-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

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...