glomerulopatia C3 komplementu C3G glomerulopatie komplementu C3 DDD MPGNII choroba denzných depozitov glomerulonefritída s hypokomplementémiou glomerulonefritída mezangiokapilárová glomerulonefritída mezangiokapilárna MPGN membranoproliferatívna glomerulonefritída MPGNII glomerulonefritída membranoproliferatívna, typ I glomerulonefritída membranoproliferatívna, typ II glomerulonefritída membranoproliferatívna, typ III glomerulonefritída mezangiokapilárna, typ I glomerulonefritída mezangiokapilárna, typ II glomerulonefritída membranoproliferatívna subendoteliálna glomerulonefritída membranoproliferatívna subendotelová MPGN, typ II glomerulonephritis membranoproliferativa glomerulonephritis mesangiocapillaris
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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