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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...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Korean Association of Orthodontists
2013
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3822065/ https://ncbi.nlm.nih.gov/pubmed/24228240 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4041/kjod.2013.43.5.248 |
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