A rare case of type 4 rapidly progressive glomerulonephritis (atypical) with mesangial IgA deposits: A case report

Rapidly progressive glomerulonephritis can result from glomerular deposition of anti-GBM antibody, immune complexes, or may involve pauci-immune mechanisms. The coexistence of IgA nephropathy, anti-GBM, and anti-neutrophilic cytoplasmic antibodies is unheard of, and the pathogenic role of these anti...

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Autores principales: Puneet Bhuwania, Ilangovan Veerappan, Ramaswami Sethuraman
Formato: article
Lenguaje:EN
Publicado: Wolters Kluwer Medknow Publications 2021
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Acceso en línea:https://doaj.org/article/cee11fef60f74b319724d9f3a35e3dca
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