Ocular manifestation of the Alport syndrome: A case report

Abstract

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.

Keywords

• Alport syndrome
• lenticonus
• renal failure