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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Detalles Bibliográficos
Autores principales: Almalki, Abdullah H, Sadagah, Laila F, Qureshi, Mohammed, Maghrabi, Hatim, Algain, Abdulrahman, Alsaeed, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714872/
https://www.ncbi.nlm.nih.gov/pubmed/29226095
http://dx.doi.org/10.5527/wjn.v6.i6.243

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714872/
https://www.ncbi.nlm.nih.gov/pubmed/29226095
http://dx.doi.org/10.5527/wjn.v6.i6.243

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