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 SSUH2, VPS4B and SMOC2 genes have been reported as responsible for...

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Detalles Bibliográficos
Autores principales: Papagiannis, Alexandros, Fanourakis, Galinos, Mitsea, Anastasia, Karayianni, Kety, Vastardis, Heleni, Sifakakis, Iosif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234607/
https://www.ncbi.nlm.nih.gov/pubmed/34207061
http://dx.doi.org/10.3390/children8060519

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234607/
https://www.ncbi.nlm.nih.gov/pubmed/34207061
http://dx.doi.org/10.3390/children8060519

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