eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | alport syndrome |
| Comorbidity | C0035078|renal failure |
| Sentences | 4 |
| PubMedID- 25165179 | The hereditary type iv collagen disease alport syndrome (as) always leads to end-stage renal failure. |
| PubMedID- 20221644 | A 61-year-old woman with chronic renal failure (crf) associated with alport syndrome underwent coronary artery aneurysmectomy under general anesthesia. |
| PubMedID- 20428923 | In addition, α3(iv), α4(iv) or α5(iv) mutations cause alport syndrome, which leads to renal failure, deafness and retinopathy in patients [27, 88, 89]. |
| PubMedID- 25649157 | Lenticonus and central fleck retinopathy strongly suggest the diagnosis of alport syndrome and are associated with renal failure before the age of 30 years, in males with x-linked disease. |
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