Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

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Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

Recent advances show that human focal segmental glomerulosclerosis (FSGS) is a primary podocytopathy caused by podocyte-specific gene mutations including NPHS1, NPHS2, WT-1, LAMB2, CD2AP, TRPC6, ACTN4 and INF2. This review focuses on genes discovered in the investigation of complex FSGS pathomechanisms that may have implications for the current FSGS classification scheme. It also recounts recen...

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Focal Segmental Glomerulosclerosis: Genetics, Mechanism, and Therapies

1Department of Internal Medicine IV (Nephrology and Hypertension), Medical University Innsbruck, Anichstraße 35, 6020 Innsbruck, Austria 2Pediatric Nephrology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany 3Department of Microbiology and Immunology, KU Leuven and Department of Nephrology, UZ Leuven, 3000 Leuven, Belgium 4Department of Pediatric Nephrology, Severance Childr...

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Focal Segmental Glomerulosclerosis.

Focal segmental glomerulosclerosis (FSGS) is a leading cause of kidney disease worldwide. The presumed etiology of primary FSGS is a plasma factor with responsiveness to immunosuppressive therapy and a risk of recurrence after kidney transplant-important disease characteristics. In contrast, adaptive FSGS is associated with excessive nephron workload due to increased body size, reduced nephron ...

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ژورنال

عنوان ژورنال: BMC Nephrology

سال: 2015

ISSN: 1471-2369

DOI: 10.1186/s12882-015-0090-9