Atypical hemolytic uremic syndrome: from diagnosis to treatment

Author:

Franchini Massimo

Abstract

AbstractThrombotic microangiopathy (TMA) is a relatively rare condition but a medical urgency requiring immediate intervention to avoid irreversible organ damage or death. Symptoms on presentation include microangiopathic haemolytic anaemia, thrombocytopenia and organ damage. The most frequent direct causes of TMA are thrombotic thrombocytopenic purpura (TTP) and haemolytic uremic syndrome (HUS). The most common form of HUS is related to Shiga toxin producing

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Reference124 articles.

1. de Gain - of - function mutations in complement factor are associated with atypical hemolytic uremic syndrome;Goicoechea;Proc Natl Acad Sci USA,2007

2. kidney transplantation to cure atypical still an option post - eculizumab;Saland;Liver Pediatr Nephrol,2014

3. Study Group for Atypical HUS for atypical hemolytic uremic syndrome recurrence in renal transplantation;Zuber;Am J Transplant,2012

4. European Paediatric Study Group for HUS Guideline for the investigation and initial therapy of diarrhea - negative hemolytic uremic syndrome;Ariceta;Pediatr Nephrol,2009

5. MA by toxin producing coli an overview;Karmali;Infection Mol Biotechnol,2004

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