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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
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 |
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