Still disease is a polygenic disorder the genes that seem to contribute include LACC1, IL6, and MIF. It is characterized by juvenile arthritis accompanied by extra-articular manifestations such as fever and cutaneous eruptions.
| 1. |
Rooney M et. al. (1995) Inflammatory cytokine responses in juvenile chronic arthritis.
|
| 3. |
Donn RP et. al. (2001) A novel 5'-flanking region polymorphism of macrophage migration inhibitory factor is associated with systemic-onset juvenile idiopathic arthritis.
|
| 5. |
De Benedetti F et. al. (2003) Functional and prognostic relevance of the -173 polymorphism of the macrophage migration inhibitory factor gene in systemic-onset juvenile idiopathic arthritis.
|
| 6. |
Wallace CA et. al. (1991) Juvenile rheumatoid arthritis: outcome and treatment for the 1990s.
|
| 7. |
Symmons DP et. al. (1996) Pediatric rheumatology in the United Kingdom: data from the British Pediatric Rheumatology Group National Diagnostic Register.
|
| 8. |
Glass DN et. al. (1999) Juvenile rheumatoid arthritis as a complex genetic trait.
|
| 9. |
Thorne JE et. al. (2007) Juvenile idiopathic arthritis-associated uveitis: incidence of ocular complications and visual acuity loss.
|