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This case report discusses the orthodontic treatment of a 23-year-old male patient with cleidocranial dysplasia (CCD), a rare genetic condition caused by mutations in the RUNX2 gene. The patient presented with multiple dental anomalies, including impacted teeth and supernumerary teeth, which required a combination of surgical and orthodontic interventions to achieve optimal dental alignment. The report emphasizes the importance of early diagnosis and a multidisciplinary approach in managing the complex dent
- Author
- rituraj.gautom1997
- Language
- EN