Authors
Liron Livny, Ester Maor-Sagie, Rawan Daher, Orit Soffer, Noa Berar-Yanai, Rinat Gabbay Ben-Ziv
Published in
Harefuah. Volume 166. Issue 9. Pages 586-589.
Abstract
Atypical hemolytic uremic syndrome (aHUS) is a rare thrombotic microangiopathy (TMA) characterized by hemolysis, thrombocytopenia, and renal impairment, most commonly driven by complement system dysregulation. Differentiating aHUS from other conditions, such as HELLP syndrome and thrombotic thrombocytopenic purpura (TTP), is critical, particularly in pregnancy.
PMID:
42892718
Bibliographic data and abstract were imported from PubMed on 18 Oct 2026.
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