eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | membranoproliferative glomerulonephritis |
| Comorbidity | C0017658|glomerulonephritis |
| Sentences | 5 |
| PubMedID- 21288559 | In 10 cases (55%), there was coexistent glomerular pathology: 5 of these cases, including glomerulonephritis with membranoproliferative glomerulonephritis-like pattern of injury (n = 4) and membranous nephropathy (n = 1), featured deposition of immune complexes; 2 demonstrated deposition of monoclonal immunoglobulin components: lambda light chain amyloidosis (n = 1) and light chain deposition disease (n = 1); 2 showed minimal change disease; and, in 1 case, there was focal crescentic pauci-immune-type glomerulonephritis. |
| PubMedID- 21046168 | Four years after renal transplantation, immune complex glomerulonephritis with an mpgn pattern recurred in the renal graft resulting in proteinuria and progressive renal insufficiency. |
| PubMedID- 21252520 | glomerulonephritis resembling mpgn type ii has occurred spontaneously in pigs that have a genetic deficiency of the complement control protein factor h. |
| PubMedID- 22661128 | Between 1970 and 2010, etiology, pathogenesis, clinicopathological correlations, and classification were established for renal diseases as diverse as lupus nephritis [42, 43], post-infectious glomerulonephritis [44], multiple forms of membranoproliferative glomerulonephritis [45], anti-gbm disease [46, 47], membranous glomerulopathy [48–50], iga nephropathy [51–53], anca-associated vasculitis and glomerulonephritis [54–56], focal segmental glomerulosclerosis and other podocytopathies [57–59], hereditary renal diseases [47], hemolytic uremic syndrome [60], tubulointerstitial disease [61], renal injury in the kidney transplant patient [62], and many others (table 1). |
| PubMedID- 24733356 | The most common pattern of glomerular involvement in our series was glomerulonephritis with mpgn-like patterns. |
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