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Tooth formation and eruption - lessons learnt from cleidocranial dysplasia
1Section of Pediatric Dentistry and Clinical Genetics, Department of Odontology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Cleidocranial dysplasia (CCD), a genetic condition affecting teeth, causes supernumerary teeth and eruption issues. Early intervention involving tooth extraction and surgical exposure improves permanent tooth eruption.
Area of Science:
- Genetics
- Developmental Biology
- Dentistry
Background:
- Tooth formation, renewal, and eruption are complex processes.
- Genetic aberrations can significantly impact dental development.
- Cleidocranial dysplasia (CCD) is a genetic disorder affecting tooth development due to RUNX2 gene mutations.
Purpose of the Study:
- To discuss the principles of tooth formation, renewal, and eruption.
- To highlight the role of RUNX2 in dental development and eruption.
- To evaluate the long-term validity of a proposed early treatment strategy for CCD patients.
Main Methods:
- Review of clinical studies, animal models, and molecular biology research on RUNX2 and CCD.
- Analysis of a proposed treatment strategy for CCD involving early dental interventions.
- Comparison of the proposed strategy with other treatment protocols.
Main Results:
- RUNX2 is crucial for osteoblast differentiation, dental lamina regression, and osteoclastogenesis.
- CCD dental phenotype includes supernumerary teeth and delayed/arrested permanent tooth eruption.
- The proposed early treatment strategy (extraction, surgical exposure) appears valid and reduces patient care burden.
Conclusions:
- RUNX2 mutations are central to the dental anomalies observed in Cleidocranial Dysplasia.
- An early, proactive treatment approach for CCD patients is effective in managing dental complications.
- The Jensen & Kreiborg treatment strategy remains a viable and beneficial option for CCD management.
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