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Atypical Hemolytic Uremic Syndrome Caused by a Rare Complement Factor B Mutation
Thrombotic microangiopathy (TMA), a rare and diagnostically challenging condition, commonly presents with a triad of thrombocytopenia, hemolytic anemia, and end-organ damage, such as renal failure. Most cases of the hemolytic uremic syndrome (HUS) are mediated by Shiga toxin-producing Escherichia co...
Autor principal: | Bandaru, Sai Samyuktha |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934198/ https://www.ncbi.nlm.nih.gov/pubmed/35317246 http://dx.doi.org/10.7759/cureus.23207 |
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