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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Detalles Bibliográficos
Autores principales: Park, Tina Keun Nan, Vargervik, Karin, Oberoi, Snehlata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Orthodontists 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822065/
https://www.ncbi.nlm.nih.gov/pubmed/24228240
http://dx.doi.org/10.4041/kjod.2013.43.5.248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822065/
https://www.ncbi.nlm.nih.gov/pubmed/24228240
http://dx.doi.org/10.4041/kjod.2013.43.5.248

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