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...

ver descrição completa

Detalhes bibliográficos

Principais autores:	Maryam Saleem, Sana Shaikh, Zheng Hu, Nicola Pozzi, Anuja Java
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Frontiers Media S.A. 2022-05-01
coleção:	Frontiers in Immunology
Assuntos:	thrombotic microangiopathy kidney transplantation complement factor I membranous nephropathy atypical hemolytic uremic syndrome complement functional analysis
Acesso em linha:	https://www.frontiersin.org/articles/10.3389/fimmu.2022.909503/full
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!