Orthodontic and surgical management of cleidocranial dysplasia
Cleidocranial dysplasia (CCD), an autosomal dominant disorder with a prevalence of 1 in 1,000,000 individuals, is mainly caused by mutations in Runx2, a gene required for osteoblastic differentiation. It is generally characterized by hypoplastic clavicles, narrow thorax, and delayed or absent fontan...
| Main Authors: | , , |
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| Format: | Online |
| Language: | English |
| Published: |
Korean Association of Orthodontists
2013
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822065/ |