Cleidocranial dysplasia. A molecular and clinical review.

Cleidocranial dysplasia

Keywords: Cleidocranial dysplasia, RUNX2 gene, supernumerary teeth


Cleidocranial dysplasia (CCD) is a rare autosomal dominant disorder characterized by skeletal and dental abnormalities primarily, short stature, aplasia or hypoplasia of clavicles, open fontanelles and supernumerary teeth. Heterozygous mutations of the runt related transcription factor 2 (RUNX2) gene have been found in approximately 60-70% of cases leaving a large number of cases with no defined genetic cause which led us to delve into molecular mechanisms underlying CCD and thus to detect potential target genes to be explored in these patients. In this review we also highlight very broadly the phenotypic characteristics of previously reported patients with CCD.


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How to Cite
Avendaño, A., Cammarata-Scalisi, F., Rizal, M. F., Budiardjo, S. B., Suharsini, M., Fauziah, E., Grande, N. M., Fortunato, L., Plotino, G., Yavuz, İzzet, & Callea, M. (2018). Cleidocranial dysplasia. A molecular and clinical review. International Dental Research, 8(1), 35-38.