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Anti-factor H autoantibody-associated hemolytic uremic syndrome: the earlier diagnosed and treated, the better.

Abstract
Atypical hemolytic uremic syndrome (HUS) secondary to anti-factor H autoantibodies has a poor prognosis. The study by Sinha et al. of a large cohort of Indian children makes a substantial contribution to improved management of this form of HUS by showing that standardized titration of anti-factor H autoantibodies is applicable worldwide and that early treatment initiation and guidance of maintenance treatment by autoantibody titer monitoring significantly improve outcomes.
AuthorsChantal Loirat, Véronique Frémeaux-Bacchi
JournalKidney international (Kidney Int) Vol. 85 Issue 5 Pg. 1019-22 (May 2014) ISSN: 1523-1755 [Electronic] United States
PMID24786877 (Publication Type: Journal Article, Comment)
Chemical References
  • Autoantibodies
  • Blood Proteins
  • CFHR1 protein, human
  • CFHR3 protein, human
  • Complement C3b Inactivator Proteins
  • Immunosuppressive Agents
Topics
  • Autoantibodies (blood)
  • Blood Proteins (immunology)
  • Complement C3b Inactivator Proteins (immunology)
  • Female
  • Hemolytic-Uremic Syndrome (therapy)
  • Humans
  • Immunosuppressive Agents (therapeutic use)
  • Male
  • Plasma Exchange
  • Time-to-Treatment

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