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Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN.
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Authors: Yvonne B D'souza, Carolyn J P Jones, Colin D Short, Ian S D Roberts, Richard E Bonshek
Kidney international 2009 AprAuthors: Christoph Licht, Veronique Fremeaux-Bacchi
Thrombosis and haemostasis 2009 FebThought leaders and organizations working on research involving membranoproliferative glomerulonephritis.
conditions: Membranoproliferative Glomerulnephritis
interventions: Rituximab
conditions: Dense Deposit Disease
interventions: Sulodexide
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