Dense deposit disease

A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.

Also known as: Mesangiocapillary glomerulonephritis type 2, membranoproliferative glomerulonephritis type 2, MPGN 2, glomerulonephritis membranoproliferative type 2, membranoproliferative glomerulonephritis type II

27 clinical trials for this condition and its sub-types.