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Clinical and Radiological Spectrum in Cleidocranial Dysplasia: A Case Series
Fakir Mohan Debta1, Kunal Agarwal1, Basudha Bera1
1Department of Oral Medicine and Radiology, SCB Dental College and Hospital, Cuttack, Odisha, Indi.
Cleidocranial dysplasia (CCD), a genetic disorder affecting bone development due to RUNX2 mutations, presents diverse skeletal and dental abnormalities. Early diagnosis of these manifestations is crucial for improving patient outcomes and quality of life.
Area of Science:
- Genetics
- Orthopedics
- Dentistry
Background:
- Cleidocranial dysplasia (CCD) is an autosomal dominant disorder.
- It is caused by mutations in the Runt-related transcription factor 2 (RUNX2) gene.
- CCD primarily affects bones formed by intramembranous ossification, leading to generalized bone and tooth dysplasia.
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