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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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Hlavní autoři: Park, Tina Keun Nan, Vargervik, Karin, Oberoi, Snehlata
Médium: Artigo
Jazyk:Inglês
Vydáno: Korean Association of Orthodontists 2013
Témata:
On-line přístup: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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