minimal-change nephrotic syndrome

min·i·mal-·change neph·rot·ic syn·drome

nephrotic syndrome with minimal glomerular changes by light or electron microscopy, occurring most frequently in children; marked by edema, albuminuria, and an increase in cholesterol in the blood, but otherwise with fairly good renal function; tubular epithelium is vacuolated by cholesterol droplets, but the glomeruli show only that the foot processes of the glomerular epithelial cells are fused, probably secondary to the proteinuria; the cause of the increased glomerular permeability to plasma protein is unknown.
References in periodicals archive ?
Long-term outcome of biopsy-proven, frequently relapsing minimal-change nephrotic syndrome in children.
The classic prototype of NS is minimal-change nephrotic syndrome (MCNS), in which case there is no identifiable cause.
Long-term outcome of biopsyproven, frequently relapsing minimal-change nephrotic syndrome in children.
Controls included 1 male patient with known X-linked AS, 1 female patient with immunoglobulin A (IgA) nephropathy, and 2 female patients with minimal-change nephrotic syndrome.