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

Fingerprint

Oral Surgery
Dental Enamel Hypoplasia
Anodontia
Language Therapy
Pediatric Dentistry
Tooth Root
Speech Therapy
Case Management
Orthodontics
Dentistry
Radiology
Tooth
Axenfeld-Rieger syndrome
Taurodontism

Cite this

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
Dunbar, A. Craig ; McIntyre, Grant T. ; Laverick, Sean ; Stevenson, Brian. / Axenfeld-Rieger syndrome : a case report. In: Journal of Orthodontics. 2015 ; Vol. 42, No. 4. pp. 324-330.
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Dunbar, AC, McIntyre, GT, Laverick, S & Stevenson, B 2015, 'Axenfeld-Rieger syndrome: a case report', Journal of Orthodontics, vol. 42, no. 4, pp. 324-330. https://doi.org/10.1179/1465313315Y.0000000017

Axenfeld-Rieger syndrome : a case report. / Dunbar, A. Craig; McIntyre, Grant T. (Lead / Corresponding author); Laverick, Sean; Stevenson, Brian.

In: Journal of Orthodontics, Vol. 42, No. 4, 2015, p. 324-330.

Research output: Contribution to journalArticle

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AB - 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.

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DO - 10.1179/1465313315Y.0000000017

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