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Year : 2015  |  Volume : 6  |  Issue : 1  |  Page : 89-91

Ocular manifestation of the Alport syndrome: A case report

Department of Ophthalmology, Chettinad Hospital and Research Institute, Tamil Nadu, India

Correspondence Address:
Charanya Chendilnathan
A 401 Urbanville, Velachery Main Road, Velachery, Chennai - 600 042
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0975-9727.146476

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The Alport syndrome is a rare genetic disorder characterized by hematuria, sensorineural deafness, and ocular manifestations. The Alport syndrome accounts for 0.3 to 2.3% of end-stage kidney disease in young males and children. Here we report a case of the Alport syndrome, with all the characteristic features.

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