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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Bibliographic Details
Published in:Korean journal of orthodontics, Vol. 43, No. 5 (2013), p. 248-60
Main Author: Park, Tina Keun Nan
Other Involved Persons: Vargervik, Karin ; Oberoi, Snehlata
Format: electronic Article
Item Description:Date Completed 14.11.2013
Date Revised 26.02.2019
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
Copyright: From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Physical Description:Online-Ressource
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