Retinitis pigmentosa associated with autosomal dominant polycystic kidney disease

被引：1
作者：
Perng, CT [1 ]
Segasothy, M [1 ]
机构：
[1] Univ Kebangsaan Malaysia, Fac Med, Dept Med, Kuala Lumpur 56000, Malaysia
来源：
NEPHROLOGY | 1998年 / 4卷 / 1-2期
关键词：
polycystic kidney disease; retinitis pigmentosa;
D O I：
10.1046/j.1440-1797.1998.d01-5.x
中图分类号：
R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];
学科分类号：
1002 ; 100201 ;
摘要：
We report a case of a 35-year-old man with autosomal dominant polycystic kidney disease (ADPKD) who presented for the first time with end-stage renal failure. He had a long history of blurred vision and on examination had retinitis pigmentosa. To our knowledge, this is the second report on the association of retinitis pigmentosa with polycystic kidney disease.
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收藏
页码：37 / 39
页数：3
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