Membranoproliferative glomerulonephritis (NP-GN) is rare disease and has also been known as mesangiocapillary glomerulonephritis, lobular glome-rulonephritis or chonic
Hypocomplementemic glomerulonephritis, By histo-pathology, MPGN is divided into type I, II and III(variant) and MPGN type II is consi-derably less common than type I Most of the patientsith it pres-ent with nephrotic syndrome and sernm complement
may be
reduced in 70 percent of them, on electron microscopic finding, it is characterized by the pres-ence of segmental of diffuse electron dense depositis, We report a case of MPGN type II without hypocomplementemia
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