WARNING:
JavaScript is turned OFF. None of the links on this concept map will
work until it is reactivated.
If you need help turning JavaScript On, click here.
This Concept Map, created with IHMC CmapTools, has information related to: membranoproliferative GM, Type 1 pathogenesis An immune-complex GN as shown by: Hypocomplementemia Activation of classical pathway with low C3, C1q and C4 Presence of C3 and IgG in glomeruli, hepatitis C Cr 3.7mg/dL low complement UA: RBCs, RBC cast 1+ protein hepB assoctd w/ membranous nephropathy, membranoproliferative glomerulonephritis MPGN 3 types Type 1, Type 1 appearance diffuse mesegial cell proliferation ->thickend and reduplicated glmr basement mbrn, membranoproliferative glomerulonephritis MPGN aka mesangiocapillary GN, Type 2 dense deposit disease pathogenesis Unknown The electron-dense material may be lipid, possibly unsaturated fatty acids, by biochemical extraction Some patients with partial lipodystrophy, a genetic disorder of lipid metabolism, develop DDD, membranoproliferative glomerulonephritis MPGN 3 types Type 2 dense deposit disease, Type 2 dense deposit disease def Capillary wall thickening and mesangial cell proliferation associated with the presence of dense deposits within the lamina densa of the GBM, Type 1 clinical features ????, membranoproliferative glomerulonephritis MPGN e.g. Sx hepatitis C Cr 3.7mg/dL low complement UA: RBCs, RBC cast 1+ protein, Type 2 dense deposit disease feature ᢒ% hypocomplementemia, Type 1 feature ᡪ% hypocomplementemia