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.

引用

页码：37 / 39

页数：3

共 13 条

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