Axenfeld-Rieger syndrome (ARS): A review and case report.

Abstract

Axenfeld-Rieger syndrome (ARS) is a rare, autosomal dominant condition characterized by ocular, craniofacial, dental, and periumbilical abnormalities. Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome. This is a case report of a 7-year-old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. Her dental condition is described, her immediate treatment is shown, and her long-term treatment needs are discussed.

DOI: 10.1111/j.1754-4505.2010.00153.x

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Cite this paper

@article{Waldron2010AxenfeldRiegerS, title={Axenfeld-Rieger syndrome (ARS): A review and case report.}, author={Jennie M Waldron and Clare McNamara and Antonia R Hewson}, journal={Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry}, year={2010}, volume={30 5}, pages={218-22} }