IgA nephropathy has been around for sixty years and is generally incurable.
IgA nephropathy is a glomerular disease in which IgA or IgA deposits predominate in the glomerular mesangial area. The cause of the disease is not completely clear, and it is currently believed that it may be related to a variety of factors, such as infections, dietary habits and the living environment, mucosal immune function abnormalities and genetic background. Patients may have symptoms such as hematuria, proteinuria and hypertension.
At present, IgA nephropathy for sixty years usually cannot be cured, but with drug treatment can relieve symptoms and improve prognosis, but there are still big differences between individuals.
Patients with IgA nephropathy should cooperate with the treatment under the guidance of doctors to prevent multiple complications such as acute renal failure and chronic renal failure due to untimely treatment.
It is recommended that patients should consult regular hospitals in time and follow the doctor’s instructions for standardized treatment.