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CASE REPORT
Year : 2019  |  Volume : 6  |  Issue : 1  |  Page : 41-44

Dental and craniofacial anomalies associated with Axenfeld–Rieger syndrome


Department of Pedodontics and Preventive Dentistry, University College of Medical Sciences (University of Delhi) and Guru Teg Bahadur Hospital, New Delhi, India

Correspondence Address:
Amit Khatri
Department of Pedodontics and Preventive Dentistry, University College of Medical Sciences and Guru Teg Bahadur Hospital, New Delhi - 110 095
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/sjos.SJOralSci_11_18

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Axenfeld–Rieger syndrome (ARS) is a rare, autosomal dominant disorder with genetic and morphologic variability and characterized by ocular and nonocular clinical findings. Midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome. This case report describes a dental condition, immediate treatment required and a long-term treatment approach toward a patient 5-year-of-age with ARS, who presented with significant ocular and dental anomalies.


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