A rare case of Alport syndrome, atypical hemolytic uremic syndrome and Pauci-immune crescentic glomerulonephritis

BACKGROUND: Renal thrombotic microangiopathy (TMA) is occasionally seen in biopsies with pauci-immune necrotizing crescentic glomerulonephritis (PCGN). Recent study indicated that the complement activation is more prominent in the ANCA-negative glomerulonephritis. CASE PRESENTATION: We report a case...

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Detalles Bibliográficos
Autores principales: Tao, Jianling, Lieberman, Jonathan, Lafayette, Richard A., Kambham, Neeraja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291978/
https://www.ncbi.nlm.nih.gov/pubmed/30541482
http://dx.doi.org/10.1186/s12882-018-1170-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291978/
https://www.ncbi.nlm.nih.gov/pubmed/30541482
http://dx.doi.org/10.1186/s12882-018-1170-4

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