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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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| Izdano u: | World J Nephrol |
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| Glavni autori: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Baishideng Publishing Group Inc
2017
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| Teme: | |
| Online pristup: | 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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