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Axenfeld–Rieger Syndrome: Rare Case Presentation and Overview

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Journal of Maxillofacial and Oral Surgery Aims and scope Submit manuscript

Abstract

Axenfeld–Rieger syndrome (ARS) is an extremely rare autosomal dominant disorder characterized by ocular, craniofacial, dental and periumbilical abnormalities. We present a case of a 10-year-old boy. Its awareness among oral surgeons is essential for timely diagnosis and subsequent prevention of ophthalmic and systemic complications as craniofacial and dental features constitute the early recognizable symptoms of this syndrome. Systematic ophthalmic surgeries aid in relieving vision abnormalities, while symptomatic dental treatment should be provided for masticatory and esthetic rehabilitation.

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Authors and Affiliations

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Contributions

PA: Concepts; PA, KV: Design; PA: Definition of intellectual content; PA, KV, SS, SC: Literature search; PA: Clinical studies; PA, SS, SC: Experimental studies; PA, SS: Data acquisition; SC: Data analysis; PA, KV: Manuscript preparation; PA, KV: Manuscript editing; KV, SS, SC: Manuscript review; PA: Guarantor.

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Correspondence to Padmanidhi Agarwal.

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Patients mother’s informed written consent was obtained for use of patient’s photographs and details for academic purpose. The procedures followed were in accordance with the ethical standards on human experimentation and complied with the Helsinki Declaration.

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Agarwal, P., Jain, K., Sandesh, S. et al. Axenfeld–Rieger Syndrome: Rare Case Presentation and Overview. J. Maxillofac. Oral Surg. 19, 364–369 (2020). https://doi.org/10.1007/s12663-019-01307-9

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  • DOI: https://doi.org/10.1007/s12663-019-01307-9

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