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Atypical hemolytic uremic syndrome: a syndrome in need of clarity
Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA) originally understood to be limited to renal and hematopoietic involvement. Whereas aberrations in complement regulatory proteins (CRPs), C3 or complement factor B (CFB) are detected in ∼60% of patients, a complement-der...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543964/ https://www.ncbi.nlm.nih.gov/pubmed/31198222 http://dx.doi.org/10.1093/ckj/sfy066 |