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FSGS: Diagnosis and Diagnostic Work-Up

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 h...

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Detalles Bibliográficos
Autores principales: Sprangers, Ben, Meijers, Björn, Appel, Gerald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894996/
https://www.ncbi.nlm.nih.gov/pubmed/27314022
http://dx.doi.org/10.1155/2016/4632768
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author Sprangers, Ben
Meijers, Björn
Appel, Gerald
author_facet Sprangers, Ben
Meijers, Björn
Appel, Gerald
author_sort Sprangers, Ben
collection PubMed
description 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 biomarkers to 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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spelling pubmed-48949962016-06-16 FSGS: Diagnosis and Diagnostic Work-Up Sprangers, Ben Meijers, Björn Appel, Gerald Biomed Res Int Review Article 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 biomarkers to 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. Hindawi Publishing Corporation 2016 2016-05-24 /pmc/articles/PMC4894996/ /pubmed/27314022 http://dx.doi.org/10.1155/2016/4632768 Text en Copyright © 2016 Ben Sprangers et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Sprangers, Ben
Meijers, Björn
Appel, Gerald
FSGS: Diagnosis and Diagnostic Work-Up
title FSGS: Diagnosis and Diagnostic Work-Up
title_full FSGS: Diagnosis and Diagnostic Work-Up
title_fullStr FSGS: Diagnosis and Diagnostic Work-Up
title_full_unstemmed FSGS: Diagnosis and Diagnostic Work-Up
title_short FSGS: Diagnosis and Diagnostic Work-Up
title_sort fsgs: diagnosis and diagnostic work-up
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894996/
https://www.ncbi.nlm.nih.gov/pubmed/27314022
http://dx.doi.org/10.1155/2016/4632768
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