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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| Auteurs principaux: | , , |
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| Format: | article |
| Langue: | EN |
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Wolters Kluwer Medknow Publications
2021
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| Accès en ligne: | https://doaj.org/article/cee11fef60f74b319724d9f3a35e3dca |
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