作者
Christophe Legendre,Christoph Licht,Petra Muus,Larry A. Greenbaum,Sunil Babu,Camille L. Bedrosian,Coralie Bingham,D.J. Cohen,Yahsou Delmas,K. Douglas,Frank Eitner,Thorsten Feldkamp,Denis Fouque,Richard R. Furman,Osama Gaber,Maria Herthelius,Maryvonne Hourmant,Diana Karpman,Yvon Lebranchu,Christophe Mariat,Jan Menne,Bruno Moulin,Jens Nürnberger,Masayo Ogawa,Giuseppe Remuzzi,Tristan Richard,Rébecca Sberro‐Soussan,Beth Severino,N. Sheerin,Antonella Trivelli,Lothar Bernd Zimmerhackl,Tim Goodship,Chantal Loirat
摘要
Atypical hemolytic–uremic syndrome is a genetic, life-threatening, chronic disease of complement-mediated thrombotic microangiopathy. Plasma exchange or infusion may transiently maintain normal levels of hematologic measures but does not treat the underlying systemic disease.
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