Axenfeld-Rieger syndrome: a case report

A. Craig Dunbar, Grant T. McIntyre (Lead / Corresponding author), Sean Laverick, Brian Stevenson

Research output: Contribution to journalArticle

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.

Original languageEnglish
Pages (from-to)324-330
Number of pages7
JournalJournal of Orthodontics
Volume42
Issue number4
DOIs
Publication statusPublished - 2015

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    Dunbar, A. C., McIntyre, G. T., Laverick, S., & Stevenson, B. (2015). Axenfeld-Rieger syndrome: a case report. Journal of Orthodontics, 42(4), 324-330. https://doi.org/10.1179/1465313315Y.0000000017