Atypical hemolytic-uremic syndrome due to complement factor I mutation

Atypical hemolytic-uremic syndrome (aHUS) is a rare disease of complement dysregulation leading to thrombotic microangiopathy (TMA). Renal involvement and progression to end-stage renal disease are common in untreated patients. We report a 52-year-old female patient who presented with severe acute k...

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Bibliografiske detaljer
Udgivet i:World J Nephrol
Main Authors: Almalki, Abdullah H, Sadagah, Laila F, Qureshi, Mohammed, Maghrabi, Hatim, Algain, Abdulrahman, Alsaeed, Ahmed
Format: Artigo
Sprog:Inglês
Udgivet: Baishideng Publishing Group Inc 2017
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5714872/
https://ncbi.nlm.nih.gov/pubmed/29226095
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5527/wjn.v6.i6.243
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