Ocular manifestation of the Alport syndrome: A case report
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 characteristi...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Wolters Kluwer Medknow Publications,
2015-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | 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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| Item Description: | 0975-9727 10.4103/0975-9727.146476 |