In children, the most common cause of nephrotic syndrome is idiopathic nephrotic syndrome (INS), also called nephrosis (1). INS is defined by the combination of a nephrotic syndrome (proteinuria, hypoalbuminemia, hyperlipidemia, and edema) and non-specific histological abnormalities of the kidney including minimal changes, focal and segmental glomerular sclerosis (FSGS), and diffuse mesangial proliferation. Glomeruli show a fusion of epithelial cell foot processes on electron microscopy and no significant deposits of immunoglobulins or complement on immunofluorescence.
CITATION STYLE
Niaudet, P., & Boyer, O. (2009). Idiopathic Nephrotic Syndrome in Children: Clinical Aspects. In Pediatric Nephrology (pp. 667–702). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-540-76341-3_28
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