Copyright: ©Author(s) 2026.
World J Transl Med. Jul 28, 2026; 12(2): 122755
Published online Jul 28, 2026. doi: 10.5528/wjtm.122755
Published online Jul 28, 2026. doi: 10.5528/wjtm.122755
Table 2 Pre-test counselling framework for genetic testing in glomerular hematuria
| Counselling topic | Standard patient-facing counselling script |
| Why the test is being done? | This test looks for differences in your genes that can cause kidney disease. We are checking these differences to see if they can explain your symptoms and help us determine best way to care for you |
| What the results may show? | |
| Positive - pathogenic/Likely pathogenic | This means we found a genetic difference that causes disease and explains your condition |
| Negative - benign/Likely benign | This means no known disease- causing difference was found. It doesn't always rule out a genetic cause, but we didn’t find one today |
| Inconclusive | We found a genetic difference, but we aren’t sure yet if it’s the cause of the disease or just a normal variation |
| So what’s next? How it affects treatment or family | Finding a genetic cause can change your treatment plan, such as suggesting different medication or extra screenings. Because this condition runs in the family it may also help us identify if your relatives are at risk |
- Citation: Bashyam S, Shankar M. Beyond the bladder: Recognising glomerular hematuria and the role of genetic testing in clinical practice. World J Transl Med 2026; 12(2): 122755
- URL: https://www.wjgnet.com/2220-6132/full/v12/i2/122755.htm
- DOI: https://dx.doi.org/10.5528/wjtm.122755