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Atypical haemolytic uraemic syndrome with underlying glomerulopathies. A case series and a review of the literature.

Authors
  • Manenti, Lucio
  • Gnappi, Elisa
  • Vaglio, Augusto
  • Allegri, Landino
  • Noris, Marina
  • Bresin, Elena
  • Pilato, Francesco Paolo
  • Valoti, Elisabetta
  • Pasquali, Sonia
  • Buzio, Carlo
Type
Published Article
Journal
Nephrology Dialysis Transplantation
Publisher
Oxford University Press
Publication Date
Sep 01, 2013
Volume
28
Issue
9
Pages
2246–2259
Identifiers
DOI: 10.1093/ndt/gft220
PMID: 23787552
Source
Medline
Keywords
License
Unknown

Abstract

Different types of glomerulopathies can be complicated by aHUS. Several mechanisms can contribute to this association, such as nephrotic-range proteinuria, mutations or aHUS-risk haplotypes involving genes encoding alternative complement regulatory proteins in some patients and inflammatory triggers associated with systemic immune-mediated diseases.

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