Results Nephrotic syndrome was the most common clinical manifestation(30.9%),followed by simple hematuria(25.5%),hematuria with proteinuria(23.6%),acute nephritic syndrome((18.2%)) and chronic nephritic syndrome(1.8%).
Twenty-six patients with nephrotic syndrome were enrolled in this study.
The intensity of luminal cubilin and tubular accumulation of albumin were significantly increased in nephrotic kidneys.
Cubilin was required for handling a greater amount of protein in nephrotic status and albumin-induced production of MCP-1 and RANTES by renal tubular cells, which further initiated tubulointerstitial inflammation in proteinuric disease.
Recurrent nephrotic syndrome in patient with multiple sclerosis treated with interferon beta-1a
We are reporting a case of pneumococcal cellulitis with bacteremia in a patient with familial Mediterranean fever (FMF) and nephrotic syndrome.
Study of interference treatment by Xuesaitong soft capsule on patients of nephrosis syndrome with Qi deficiency and blood stasis
Minimal change disease (lipoid nephrosis), (60, 12%), membranous glomerulonephritis (51, 10.2%) and focal proliferating glomerulonephritis, (excluding lupus nephritis and IgA nephropathy), (59, 11.8%) were the three most common glomerular diseases.
It is slowly reduced if the serum albumin content is markedly reduced as in protein deficiency, the blind loop syndrome, cirrhosis, nephrosis, and diseases of the gastrointestinal tract.
There is also severe glycogenic nephrosis and myocardosis and preliminary observations suggest the presence of thickening of the capillary basement membrane of the renal glomeruli and in the endocrine pancreas.
Most patients (84 %) suffered from congenital nephrosis of the Finnish type.