Absence of thrombocytopaenia and/or microangiopathic haemolytic anaemia does not reliably exclude recurrence of atypical haemolytic uraemic syndrome after kidney transplantation

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Absence of thrombocytopaenia and/or microangiopathic haemolytic anaemia does not reliably exclude recurrence of atypical haemolytic uraemic syndrome after kidney transplantation

© 2017 Asian Pacific Society of NephrologyA 54-year-old man was diagnosed with atypical haemolytic uraemic syndrome (aHUS) with confirmed complement H mutation in 2012, requiring ongoing dialysis. He was commenced on eculizumab in 2014 once the pharmaceutical board approved this drug. After 4 months...

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Bibliographic Details
Main Authors:	Krishnan, A., Siva, B., Chakera, Aron, Wong, G., Wong, D., Lim, W.
Format:	Journal Article
Published:	Wiley-Blackwell 2017
Online Access:	http://hdl.handle.net/20.500.11937/52002

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