eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | alport syndrome |
| Symptom | C0033687|proteinuria |
| Sentences | 3 |
| PubMedID- 21688191 | In contrast, the much rarer homozygous or compound heterozygous of such mutations in the col4a3/col4a4 genes develop the classical autosomal recessive alport syndrome course with early proteinuria and hypertension, reaching eskd by late adolescence and the early 20s. |
| PubMedID- 20238228 | Based on these results, we suggest that csa is effective in reducing proteinuria in patients with alport syndrome but that this effect is temporary. |
| PubMedID- 23207876 | Losartan and enalapril are comparable in reducing proteinuria in children with alport syndrome. |
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