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...

Full description

Saved in:
Bibliographic Details
Published in01173f6b-d01d-49c3-b18e-93cfe3a0383d pp. 471 - 483
Format Book Chapter
LanguageEnglish
Published Exon Publications 18.11.2015
Subjects
acute kidney injury
Autosomal Dominant Polycystic Kidney Disease
MJR
Rapidly Progressive Glomerulonephritis
Online AccessGet full text

Cover

Abstract 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.
AbstractList 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.
BookMark eNotj9FKwzAUQAMq6Ob-YA_5gdabLunSx7HpJg4cMnwdt0nq4trc0nRC_96CPp2HAwfOhN0GCo6xuYBUKKXzJ0OWQtpebJqBUKk5Z3DDJlAUUi60gOKezWL8BoBR6wLkA_v8wNbbeuCHjr46F6P_cXxbU-O6az3W23Pnex-5D3x17SlSgzXfUOMDhp4fqB7MEHtv-Ju3wQ1846PD6B7ZXYV1dLN_Ttnx5fm43iX79-3rerVPSEDeJ8s8N6qspFGgylzqDDVUkBkn5SiUUCUKUMJZYaWyRVFWqDRaNKA1LqvFlM3_soStCydLWBJd4kmMt8t88QusIFVX
ContentType Book Chapter
DBID V1H
DOI 10.15586/codon.pkd.2015.ch20
DatabaseName DOAB: Directory of Open Access Books
DatabaseTitleList
Database_xml – sequence: 1
  dbid: V1H
  name: DOAB: Directory of Open Access Books
  url: https://directory.doabooks.org/
  sourceTypes: Publisher
DeliveryMethod fulltext_linktorsrc
EndPage 483
ExternalDocumentID 138176
GroupedDBID ALMA_UNASSIGNED_HOLDINGS
CZQ
V1H
ID FETCH-LOGICAL-o106t-766c5bf4c505b6482a80f02ce446c5515ba1051ed1d45d99bfa58adac088a7f3
IEDL.DBID V1H
ISBN 0994438109
9780994438102
IngestDate Fri Oct 11 15:19:10 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed false
IsScholarly false
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-o106t-766c5bf4c505b6482a80f02ce446c5515ba1051ed1d45d99bfa58adac088a7f3
OpenAccessLink https://directory.doabooks.org/handle/20.500.12854/138176
PageCount 13
ParticipantIDs oapen_doabooks_138176
PublicationCentury 2000
PublicationDate 2015-11-18
PublicationDateYYYYMMDD 2015-11-18
PublicationDate_xml – month: 11
  year: 2015
  text: 2015-11-18
  day: 18
PublicationDecade 2010
PublicationTitle 01173f6b-d01d-49c3-b18e-93cfe3a0383d
PublicationYear 2015
Publisher Exon Publications
Publisher_xml – name: Exon Publications
SSID ssj0002018904
Score 1.5072355
Snippet Patients with autosomal dominant polycystic kidney disease (ADPKD) can suffer from the same causes of acute kidney injury as the general population. Affected...
SourceID oapen
SourceType Publisher
StartPage 471
SubjectTerms acute kidney injury
Autosomal Dominant Polycystic Kidney Disease
MJR
Rapidly Progressive Glomerulonephritis
Title Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
URI https://directory.doabooks.org/handle/20.500.12854/138176
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwdV1NT8JAEN0oXIwXjRi_swevxX7slt2jEZFoYohBwo3sVyOxdAkUk_57Z1owXDy2p3Zms_Nm9703hNxLx1InFQ-yTCUBQxtC6TgPHHQbYaIsk1nNtnhPh5_sdcqne6O-mo3cI6vZK8SZ6_o6v7EcgE69y0N0RBCcPURoLpcekjbnUNRhKU-i4d_xCtQ1IUMc6gQQiNU-VnLrt7N7jrdKOs5FigJyyPryG81DI941XzgAvO3V0hV79WZwQo5Rg0BRHAD_fUoOXHFGJh9qObd5RUfIqUL66o-jL7lfuNUm94WDtKBBEZ0X9HFT-rVfqJz2fcN1oSOfV6ZCV2b6NreFq2i_uZvpkPHgefw0DLZjEQIP_VsZ9NLUcJ0xA-BFp0zESoRZGBsHnZ0BAMS1AtAUORtZxq2UOlNcKKsMbCiqlyXnpFXAR10QapgViRI9I9BmPjKKSe2gYYyUFjrW7JJ06gjMdrmYNTG_-uf9NTnC6KFULxI3pFWuNu4Wanap7-rs_ALCeJIj
link.rule.ids 782,783,787,796,27939,55644
linkProvider Open Access Publishing in European Networks
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=bookitem&rft.title=01173f6b-d01d-49c3-b18e-93cfe3a0383d&rft.atitle=Rapidly+Progressive+Glomerulonephritis+in+Autosomal+Dominant+Polycystic+Kidney+Disease&rft.date=2015-11-18&rft.pub=Exon+Publications&rft.isbn=9780994438102&rft.spage=471&rft.epage=483&rft_id=info:doi/10.15586%2Fcodon.pkd.2015.ch20&rft.externalDBID=V1H&rft.externalDocID=138176
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=9780994438102/lc.gif&client=summon&freeimage=true
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=9780994438102/mc.gif&client=summon&freeimage=true
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=9780994438102/sc.gif&client=summon&freeimage=true