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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Wolters Kluwer Medknow Publications,
2015-01-01T00:00:00Z.
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A1234.567 |
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| Kopie 1 | Beschikbaar |