There are more causes of nephrotic syndrome, the prognosis varies greatly, and there is no specific data on the probability of nephrotic syndrome developing into uremia.
Nephrotic syndrome is characterized by massive proteinuria, hypoalbuminemia, edema, and hyperlipidemia, and its common causes include microscopic lesion nephropathy, proliferative nephritis of the thylakoid membrane, focal segmental glomerulosclerosis, and membranous nephropathy.
Generally speaking, patients who are sensitive to hormone and/or immunosuppressant therapy, with less severe pathology and fewer complications, have a lower probability of developing uremia; patients who are not sensitive to therapy, with more severe pathology and more complications have a much higher probability of progressing to uremia.
Patients with nephrotic syndrome should go to the hospital in time and be treated under the guidance of professional physicians.