Thrombomodulin mutations in atypical hemolytic-uremic syndrome.
Published in The New England journal of medicine • Jul 23, 2009
Authors:,,
Mieke Delvaeye
Marina Noris
Astrid De Vriese
Abstract
BACKGROUND: The hemolytic-uremic syndrome consists of the triad of microangiopathic hemolytic anemia, thrombocytopenia, and renal failure. The common form of the syndrome is triggered by infection with Shiga toxin-producing bacteria and has a favorable outcome. The less common form of the syndrome, ...
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