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...

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Detalles Bibliográficos
Autor principal: Bandaru, Sai Samyuktha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Internal Medicine
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

Internet

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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