Alport Syndrome: case report and review of ocular manifestations

被引：0
|
作者：
Jain, Charu [1 ]
Malik, V. K. [1 ]
Kamboj, Reny [1 ]
Kumar, Sanjeev [1 ]
Kumar, Sandeep [1 ]
Jain, Kirti [1 ]
机构：
[1] Subharti Inst Med Sci, Dept Ophthalmol, Delhi Haridwar Bypass Rd NH 58, Meerut, UP, India
来源：
NEPALESE JOURNAL OF OPHTHALMOLOGY | 2011年 / 3卷 / 02期
关键词：
Alport Syndrome; hereditary nephritis; lenticonus; deafness; retinopathy;
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
Background: Alport Syndrome is an uncommon disease. Case: We report a case of a young Indian male who presented with the characteristic ocular findings and systemic features of Alport Syndrome. Conclusion: Any young patient with a chronic renal disease should have a careful ophthalmologic examination for Alport Syndrome.
引用
收藏
页码：188 / 190
页数：3
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