Table 4.
Initial diagnosis, treatment and time to diagnosis
| Case | Initial diagnosis | Treatment | Time to diagnosis (years) |
|---|---|---|---|
| 1 | ITP and glomerulonephritis | CS | 23 |
| 2 | Hereditary nephropathy | 0 | 0 |
| 3 | FSGS | CS, CPA | 29 |
| 4 | ITP | CS, IVIg | 1 |
| 5 | Hereditary nephropathy | 0 | 2 |
| 6 | Glomerulonephritis | 0 | 19 |
| 7 | May–Hegglin anomaly | 0 | 0 |
| 8 | ITP | IVIg | 5 |
| 9 | ITP | CS, IVIg, splenectomy | 10 |
| 10 | May–Hegglin anomaly | 0 | 0 |
| 11 | Thrombocytopenia | 0 | 10 |
| 12 | Alport syndrome | 0 | 3 |
| 13 | Cortical necrosis | Antifibrinolytics | 1 |
CPA, cyclophosphamide; CS, corticosteroids; FSGS, focal segmental glomerulosclerosis; ITP, idiopathicthrombocytopenic purpura; IVIg, intravenous immunoglobulins.