IgA nephropathy involves IgA antibody deposition in glomeruli, causing inflammation and potential kidney damage.
Common symptoms include hematuria, proteinuria, and hypertension, though some patients may be asymptomatic.
Asymptomatic cases are frequently diagnosed incidentally during routine examinations, highlighting the disease's insidious nature.
No distinct clinical subtypes are widely recognized, but variability in progression and treatment response suggests underlying heterogeneity.
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Panelists discuss how IgA nephropathy presents in patients, often remaining asymptomatic until significant progression occurs, and explore the various subtypes that exhibit distinct clinical features.