FSGS: Diagnosis and Diagnostic Work-Up

被引:33
|
作者
Sprangers, Ben [1 ,2 ]
Meijers, Bjorn [1 ,2 ]
Appel, Gerald [3 ]
机构
[1] Katholieke Univ Leuven, Dept Microbiol & Immunol, B-3000 Leuven, Belgium
[2] Univ Hosp Leuven, Dept Nephrol, B-3000 Leuven, Belgium
[3] Columbia Univ, Med Ctr, Ctr Glomerular Dis, New York, NY 10032 USA
关键词
FOCAL SEGMENTAL GLOMERULOSCLEROSIS; SOLUBLE UROKINASE RECEPTOR; PLASMINOGEN-ACTIVATOR RECEPTOR; RESISTANT NEPHROTIC SYNDROME; MINIMAL CHANGE DISEASE; STAGE RENAL-DISEASE; CLINICAL-FEATURES; COLLAPSING GLOMERULOPATHY; MORPHOMETRIC-ANALYSIS; EPITHELIAL-CELLS;
D O I
10.1155/2016/4632768
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Focal segmental glomerulosclerosis is a histologic lesion, rather than a clinical disease. FSGS is common cause of nephrotic syndrome in both adults and children worldwide. In the United States it is the most common primary glomerular disease resulting in end-stage renal disease and recent reports have suggested that its incidence might be on the rise. Currently the incidence is estimated to be 7 per million. The podocyte is the cellular target cell in FSGS and in recent years substantial insight in the pathogenesis and genetics of FSGS have accumulated. Furthermore the discovery of potential novel biomarkersto diagnose FSGS and monitor disease activity has renewed interest in this disease. In this review article we will focus on the clinical presentation and diagnosis of FSGS.
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页数:8
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