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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| Language: | English |
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Exon Publications
2024
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| Online Access: | https://directory.doabooks.org/handle/20.500.12854/138176 |
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| 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. |
| format | Online |
| id | doab-20.500.12854ir-138176 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2024 |
| publishDateRange | 2024 |
| publishDateSort | 2024 |
| publisher | Exon Publications |
| publisherStr | Exon Publications |
| record_format | ojs |
| 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 |