Ocular manifestation of the Alport syndrome: A case report
oleh: Ayyakutty Muni Raja, Siddharam S Janti, Adnan Matheen, Charanya Chendilnathan
| Format: | Article |
|---|---|
| Diterbitkan: | Wolters Kluwer Medknow Publications 2015-01-01 |
Deskripsi
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.