IgA vasculitis (Q39610): Difference between revisions
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Vasculite, com depósitos imunes dominantes de IgA1, afetando pequenos vasos (predominantemente capilares, vênulas ou arteríolas). Muitas vezes envolve pele e intestino, e frequentemente causa artrite. Pode ocorrer glomerulonefrite indistinguível da nefropatia por IgA. | |||
| description / en | description / en | ||
Vasculitis, with IgA1-dominant immune deposits, affecting small vessels (predominantly capillaries, venules, or arterioles). Often involves skin and gut, and frequently causes arthritis. Glomerulonephritis indistinguishable from IgA nephropathy may occur. | |||
Revision as of 05:05, 13 August 2026
Vasculitis, with IgA1-dominant immune deposits, affecting small vessels (predominantly capillaries, venules, or arterioles). Often involves skin and gut, and frequently causes arthritis. Glomerulonephritis indistinguishable from IgA nephropathy may occur.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 4A44.92 |
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| English | IgA vasculitis |
Vasculitis, with IgA1-dominant immune deposits, affecting small vessels (predominantly capillaries, venules, or arterioles). Often involves skin and gut, and frequently causes arthritis. Glomerulonephritis indistinguishable from IgA nephropathy may occur. |
