Orthodontic Treatment in a Patient with Cleidocranial Dysostosis
Author(s) -
Giampietro Farronato,
Cinzia Maspero,
Davide Farronato,
Silvia Gioventù
Publication year - 2008
Publication title -
the angle orthodontist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 86
eISSN - 1945-7103
pISSN - 0003-3219
DOI - 10.2319/111307-393.1
Subject(s) - medicine , supernumerary , cleidocranial dysplasia , dysostosis , aplasia , maxilla , hypoplasia , craniofacial , skull , dentistry , orthodontics , anatomy , surgery , congenital disease , psychiatry
Cleidocranial dysostosis is a rare congenital skeletal disorder, associated with clavicular hypoplasia or aplasia, delayed closure of cranial fontanels, brachycephalic skull, delayed exfoliation of primary dentition, eruption of permanent teeth, and multiple supernumerary and morphologic abnormalities of the maxilla and mandible. The disorder is caused by mutation in the CBFA1 gene, on the short arm of chromosome 6p21. The prevalence of cleidocranial dysostosis is estimated one per million, without sex or ethnic group predilection. The purpose of this paper is to describe the orthodontic treatment in a patient with cleidocranial dysostosis. Therapy may include removal of supernumerary teeth, surgical exposure of impacted teeth, and orthodontic treatment.
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