Axenfeld–Rieger syndrome: a case report. (December 2015)

• Record Type: Journal Article
• Authors: Dunbar, A. Craig; McIntyre, Grant T.; Laverick, Sean; Stevenson, Brian
• Is Part Of: Journal of orthodontics. Volume 42:Number 4(2015:Dec.)
• Page Start: 324
• Page End: 330
• Publication Date: 2015-12
• Subjects: Axenfeld Rieger syndrome -- multidisciplinary care -- orthognathic surgery -- severe hypodontia; Orthodontics -- Periodicals; 617.643005
• DOI: 10.1179/1465313315Y.0000000017
• Languages: English
• ISSNs: 1465-3125

Abstract

Abstract : Axenfeld–Rieger syndrome (ARS) is a rare autosomal dominant condition manifesting as a heterogeneous group of features. Of particular note are the ocular and craniofacial anomalies and dental features such as hypodontia, microdontia, taurodontism, enamel hypoplasia, conical-shaped teeth, shortened roots and delayed eruption. To treat cases with ARS effectively, a multidisciplinary approach is required, and this report describes the complex and long-term management of a case with input from Paediatric Dentistry, Orthodontics, Restorative Dentistry, Speech and Language Therapy, Oral and Maxillofacial Surgery and Radiology.