eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | autosomal dominant polycystic kidney disease |
| Comorbidity | C0027726|nephrotic syndrome |
| Sentences | 5 |
| PubMedID- 20429898 | There are only anecdotal case reports of autosomal dominant polycystic kidney disease associated with nephrotic syndrome, with focal segmental glomerulosclerosis being the most commonly reported histopathological diagnosis. |
| PubMedID- 21116827 | autosomal dominant polycystic kidney disease (adpkd) associated with steroid-sensitive nephrotic syndrome in childhood. |
| PubMedID- 26069794 | Among the anecdotal case reports of adpkd associated with nephrotic syndrome, focal segmental glomerulosclerosis occurs most frequently. |
| PubMedID- 22218124 | autosomal dominant polycystic kidney disease (adpkd) with nephrotic syndrome is a rare coincidence. |
| PubMedID- 23617397 | Urinary protein excretion is usually less than 1 g/day, and adpkd is rarely associated with nephrotic syndrome or rapidly progressive glomerulonephritis (rpgn). |
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