PedAM
Pediatric Disease Annotations & Medicines
| Disease | membranoproliferative glomerulonephritis |
| Phenotype | C0017658|glomerulonephritis |
| Sentences | 2 |
| PubMedID- 21288559 | Concurrent glomerular injury may be a direct result of the lymphoplasmacytic disorder through a paraprotein deposition process resulting in amyloid or monoclonal immunoglobulin deposition disease, or may be caused indirectly through immune-mediated mechanisms, as in the cases of glomerulonephritis with membranoproliferative glomerulonephritis-like pattern of injury, membranous nephropathy, and possibly minimal change disease. |
| 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). |
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