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Atypical haemolytic uraemic syndrome: a case of rare genetic mutation
Complement-mediated kidney disease has been an evolving area in the field of nephrology. Atypical haemolytic uraemic syndrome (aHUS) is a rare thrombotic microangiopathy that affects multiple organs, particularly kidneys. The disease is characterised by a triad of haemolytic anaemia, thrombocytopeni...
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| Yayımlandı: | BMJ Case Rep |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMJ Publishing Group
2021
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8327850/ https://ncbi.nlm.nih.gov/pubmed/34330731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2021-244190 |
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