Focal segmental glomerulosclerosis in association with Gitelman syndrome

被引：6

作者：

Ceri, Mevlut ^{[1
]}

Unverdi, Selman ^{[1
]}

Altay, Mustafa ^{[2
]}

Unverdi, Hatice ^{[3
]}

Kurultak, Ilhan ^{[4
]}

Yilmaz, Rahmi ^{[1
]}

Ensari, Arzu ^{[3
]}

Duranay, Murat ^{[1
]}

机构：

[1] Ankara Educ & Res Hosp, Dept Nephrol, Ankara, Turkey

[2] Ankara Educ & Res Hosp, Dept Internal Med, Ankara, Turkey

[3] Ankara Univ, Dept Pathol, Fac Med, TR-06100 Ankara, Turkey

[4] Ankara Univ, Dept Nephrol, Fac Med, TR-06100 Ankara, Turkey

来源：

INTERNATIONAL UROLOGY AND NEPHROLOGY | 2011年 / 43卷 / 03期

关键词：

Gitelman syndrome; Proteinuria; Focal segmental glomerulosclerosis; HYPOKALEMIC ALKALOSIS; EXPRESSION; KIDNEY;

D O I：

10.1007/s11255-010-9802-z

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：

Gitelman syndrome (GS) is an autosomal recessive disorder characterized by hypokalemia, metabolic alkalosis, hypomagnesemia and hypocalciuria. Glomerulonephritis associated with GS is rarely documented in the literature. We present an adult patient with GS whose renal biopsy revealed focal segmental glomerulosclerosis.

引用

页码：905 / 907

页数：3

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