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

• Asıl Yazarlar: Alexandros Papagiannis (Yazar), Galinos Fanourakis (Yazar), Anastasia Mitsea (Yazar), Kety Karayianni (Yazar), Heleni Vastardis (Yazar), Iosif Sifakakis (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: MDPI AG, 2021-06-01T00:00:00Z.
• Konular: article
• Online Erişim: 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...