SourceJournal of Orthodontics, 37, 2, (2010), pp. 121-7
01 juni 2010
Article / Letter to editor
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Journal of Orthodontics
SubjectIGMD 3: Genomic disorders and inherited multi-system disorders
This case report describes the combined orthodontic and orthognathic management of a 14-year-old girl affected with Apert syndrome. She presented with a severe Class III skeletal relationship, midfacial hypoplasia and an large anterior open bite. Intraorally, she had severe crowding, a narrow maxilla and lateral posterior crossbites. The patient was treated with a combination of removable and fixed appliances, a transpalatal skeletal distractor and Le Fort I surgery. The extraoral characteristics improved and a good occlusal relationship between maxillary and mandibular teeth was achieved.
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- Faculty of Medical Sciences 
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