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.
Also Known As:
Membranoproliferative Glomerulonephritis, Type II; Dense Deposit Disease; Mesangiocapillary Glomerulonephritis; Glomerulonephritis, Membranoproliferative; DDD MPGNII; Glomerulonephritis, Hypocomplementemic; MPGNII; Membranoproliferative Glomerulonephritis Type II; Membranoproliferative Glomerulonephritis, Type I; Membranoproliferative Glomerulonephritis, Type III; Mesangiocapillary Glomerulonephritis, Type I; Mesangiocapillary Glomerulonephritis, Type II; Subendothelial Membranoproliferative Glomerulonephritis; Type II MPGN; DDD MPGNIIs; Glomerulonephritides, MPGN Membranoproliferative; Glomerulonephritides, Membranoproliferative; Glomerulonephritis, MPGN Membranoproliferative; Glomerulopathies, Complement 3; Glomerulopathy, Complement 3; Hypocomplementemic Glomerulonephritides; Hypocomplementemic Glomerulonephritis; MPGN Membranoproliferative Glomerulonephritides; MPGN, Type II; MPGNII, DDD; MPGNIIs; Membranoproliferative Glomerulonephritides; Membranoproliferative Glomerulonephritides, MPGN; Membranoproliferative Glomerulonephritis, MPGN; Membranoproliferative Glomerulonephritis, Subendothelial; Mesangiocapillary Glomerulonephritides; Type II MPGNs; C3G Complement 3 Glomerulopathy; Complement 3 Glomerulopathies; Complement 3 Glomerulopathy; Glomerulonephritis, Mesangiocapillary; MPGN Membranoproliferative Glomerulonephritis