Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report

Background: Cleidocranial dysplasia (CCD) is a rare, autosomal dominant skeletal dysplasia with a prevalence of one per million births. The main causes of CCD are mutations in the core-binding factor alpha-1 (CBFA1) or runt-related transcription factor-2 (RUNX2), located at the 6p21 chromosomal regi...

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Detalles Bibliográficos
Autores principales: Inchingolo, Alessio Danilo, Patano, Assunta, Coloccia, Giovanni, Ceci, Sabino, Inchingolo, Angelo Michele, Marinelli, Grazia, Malcangi, Giuseppina, Montenegro, Valentina, Laudadio, Claudia, Palmieri, Giulia, Bordea, Ioana Roxana, Ponzi, Emanuela, Orsini, Paola, Ficarella, Romina, Scarano, Antonio, Lorusso, Felice, Dipalma, Gianna, Corsalini, Massimo, Gentile, Mattia, Venere, Daniela Di, Inchingolo, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709258/
https://www.ncbi.nlm.nih.gov/pubmed/34946295
http://dx.doi.org/10.3390/medicina57121350

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709258/
https://www.ncbi.nlm.nih.gov/pubmed/34946295
http://dx.doi.org/10.3390/medicina57121350

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