Pediatric nephrotic syndrome: from the simple to the complex.

Abstract:

:Remarkable advances have been made in the past decade in understanding the pathophysiology of idiopathic nephrotic syndrome. Although the initiating events leading to the onset of proteinuria still are not well defined, it has become increasingly clear that many glomerular diseases can be classified as podocytopathies, with injury to the podocyte playing a major role in the development and progression of disease. A complex interaction of immune system mediators, slit diaphragm signal transduction, podocyte injury and conformational change, and mediators of apoptosis and fibrosis determine the extent and nature of proteinuria and progression of glomerulosclerosis. New insights into the pathogenesis of idiopathic nephrotic syndrome likely will lead to innovative therapies and new approaches to management and prevention.

journal_name

Semin Nephrol

journal_title

Seminars in nephrology

authors

Lane JC,Kaskel FJ

doi

10.1016/j.semnephrol.2009.03.015

subject

Has Abstract

pub_date

2009-07-01 00:00:00

pages

389-98

issue

4

eissn

0270-9295

issn

1558-4488

pii

S0270-9295(09)00052-7

journal_volume

29

pub_type

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