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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:World J Nephrol
Main Authors: Almalki, Abdullah H, Sadagah, Laila F, Qureshi, Mohammed, Maghrabi, Hatim, Algain, Abdulrahman, Alsaeed, Ahmed
Formato: Artigo
Idioma:Inglês
Publicado em: Baishideng Publishing Group Inc 2017
Assuntos:
Case Report
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados