Abstract:Background
Atypical hemolytic uremic syndrome (aHUS) is a disorder of the microvasculature with hemolytic anemia, thrombocytopenia and acute kidney injury. Nowadays, aHUS is successfully treated with eculizumab, a humanized, chimeric IgG2/4 kappa antibody, which binds human complement C5 and blocks generation of C5a and membrane-attack-complex.
Case presentation
A 25-year-old woman with end stage renal disease due to relapsing atypical hemolytic uremic syndrome had a re… Show more
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