Post-Transplant Thrombotic Microangiopathy due to a Pathogenic Mutation in Complement Factor I in a Patient With Membranous Nephropathy: Case Report and Review of Literature

Thrombotic microangiopathy (TMA) is characterized by microangiopathic hemolytic anemia, thrombocytopenia and organ injury occurring due to endothelial cell damage and microthrombi formation in small vessels. TMA is primary when a genetic or acquired defect is identified, as in atypical hemolytic ure...

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Detalles Bibliográficos
Autores principales: Saleem, Maryam, Shaikh, Sana, Hu, Zheng, Pozzi, Nicola, Java, Anuja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204634/
https://www.ncbi.nlm.nih.gov/pubmed/35720299
http://dx.doi.org/10.3389/fimmu.2022.909503

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204634/
https://www.ncbi.nlm.nih.gov/pubmed/35720299
http://dx.doi.org/10.3389/fimmu.2022.909503

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