Objectives: Cleidocranial dysplasia (CCD) is an autosomal dominant malformation syndrome in which a mutation occurs in the RUNX2 gene on chromosome 6 and affects bone and tooth development. This article aims to describe the CBCT radiographic findings and diagnostic evaluation of a case with multiple impactions. Case Report: A 21-year-old patient came to RSGM with complaints that his teeth felt messy. The orthodontist who examined him found that there was a lot of delay in eruption, and then CBCT radiography was performed. After an examination using CBCT, it was seen that there were many impacted teeth, starting from the central incisor, left and right premolars, both. Conclusion: Cleidocranial dysplasia (CCD) is a developmental disorder characterized by delayed tooth eruption, supernumerary teeth, and clavicular abnormalities
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