Table 7.
Non-infectious, systemic disease-associated
| Diagnosis | No | Percentage | ||
| Systemic (74) | Non-infectious (184) | Total (276) | ||
| JIA | 41 | 55.4 | 22.3 | 14.9 |
| Behçet’s | 13 | 17.6 | 7.1 | 4.7 |
| TINU | 4 | 5.4 | 2.2 | 1.4 |
| Masquerade* | 4 | 5.4 | 2.2 | 1.4 |
| VKH | 3 | 4.1 | 1.6 | 1.1 |
| Sarcoidosis | 2 | 2.7 | 1.1 | 0.7 |
| Gaucher | 2 | 2.7 | 1.1 | 0.7 |
| Reiter’s disease | 2 | 2.7 | 1.1 | 0.7 |
| Spondylitis | 1 | 1.4 | 0.5 | 0.4 |
| Juvenile psoriasis | 1 | 1.4 | 0.5 | 0.4 |
| Juvenile polychondritis | 1 | 1.4 | 0.5 | 0.4 |
| Total | 74 | 100.2 | 40.2 | 26.8 |
*Three of these patients had acute lymphoblastic leukaemia (ALL) and were in remission when the “uveitis” was detected. Systemic examination disclosed a recurrence of the disease. Treatment induced remission of the systemic disease and “clearing” of the intraocular findings. The fourth case in this group had Langerhans cell histyocytosis.