Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease

Patients with autosomal dominant polycystic kidney disease (ADPKD) can suffer from the same causes of acute kidney injury as the general population. Affected individuals may present with hematuria and proteinuria (usually less than 1g/day). However, nephrotic syndrome and proliferative glomeruloneph...

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Format: Online
Language:English
Published: Exon Publications 2024
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Online Access:https://directory.doabooks.org/handle/20.500.12854/138176
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collection Directory of Open Access Books
description Patients with autosomal dominant polycystic kidney disease (ADPKD) can suffer from the same causes of acute kidney injury as the general population. Affected individuals may present with hematuria and proteinuria (usually less than 1g/day). However, nephrotic syndrome and proliferative glomerulonephritis are uncommon in patients with polycystic kidney disease. Development of nephrotic syndrome and / or rapid deterioration in kidney function suggest the presence of another, more aggressive disorder, requiring prompt diagnosis and appropriate interventions to mitigate further injury and progression to end stage kidney disease. In this chapter, we will discuss rapidly progressive glomerulonephritis in association with ADPKD.
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spelling doab-20.500.12854ir-1381762024-05-21T23:58:07Z Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease Rapidly Progressive Glomerulonephritis Autosomal Dominant Polycystic Kidney Disease acute kidney injury MJR Patients with autosomal dominant polycystic kidney disease (ADPKD) can suffer from the same causes of acute kidney injury as the general population. Affected individuals may present with hematuria and proteinuria (usually less than 1g/day). However, nephrotic syndrome and proliferative glomerulonephritis are uncommon in patients with polycystic kidney disease. Development of nephrotic syndrome and / or rapid deterioration in kidney function suggest the presence of another, more aggressive disorder, requiring prompt diagnosis and appropriate interventions to mitigate further injury and progression to end stage kidney disease. In this chapter, we will discuss rapidly progressive glomerulonephritis in association with ADPKD. Published 2024-05-21T23:58:03Z 2024-05-21T23:58:03Z 2015-11-18 chapter 978-0-9944381-0-2 https://directory.doabooks.org/handle/20.500.12854/138176 eng image/jpeg Attribution-NonCommercial-NoDerivatives 4.0 International https://exonpublications.com/index.php/exon/article/view/88 Exon Publications Polycystic Kidney Disease 10.15586/codon.pkd.2015.ch20 10.15586/codon.pkd.2015.ch20 2d6001a3-9e06-4979-bf02-6974e313eb24 01173f6b-d01d-49c3-b18e-93cfe3a0383d 978-0-9944381-0-2 471-483 open access
spellingShingle Rapidly Progressive Glomerulonephritis
Autosomal Dominant Polycystic Kidney Disease
acute kidney injury
MJR
Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
title Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
title_full Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
title_fullStr Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
title_full_unstemmed Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
title_short Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
title_sort rapidly progressive glomerulonephritis in autosomal dominant polycystic kidney disease
topic Rapidly Progressive Glomerulonephritis
Autosomal Dominant Polycystic Kidney Disease
acute kidney injury
MJR
topic_facet Rapidly Progressive Glomerulonephritis
Autosomal Dominant Polycystic Kidney Disease
acute kidney injury
MJR
url https://directory.doabooks.org/handle/20.500.12854/138176