DISEASE SCANNER
Global Incurable Diseases Tracker
Juvenile Idiopathic Arthritis
The most common chronic rheumatic disease in children, characterized by persistent joint inflammation lasting >6 weeks in children <16 years. Multiple subtypes including oligoarticular, polyarticular, and systemic (Still's disease). Can cause permanent joint damage and growth abnormalities.
3.0M
111
Symptoms
Treatment Options
Risk Factors
Diagnostic Methods
- 1Physical examination
- 2Blood tests (RF, anti-CCP, ANA, ESR, CRP)
- 3X-rays
- 4MRI or ultrasound
- 5Eye examination (slit lamp)
- 6Bone scan
Prognosis
Variable by subtype. Oligoarticular: 50-70% remission. Polyarticular: more guarded, may persist into adulthood. Systemic: challenging, macrophage activation syndrome risk. Permanent joint damage possible without early aggressive treatment.
Prevention
- No known primary prevention
- Early diagnosis and treatment
- Regular screening for uveitis
- Vaccinations before biologics
- Physical activity maintenance
- Healthy diet
Research Status
Treat-to-target approach achieving remission in 50-70%. Biologics (etanercept, adalimumab, tocilizumab, abatacept) transformative. Tofacitinib approved for polyarticular JIA. Long-acting IL-1 and IL-6 inhibitors for systemic JIA.
Affected Countries
Sources
- https://www.cdc.gov/
- https://www.hematology.org/education/patients
- https://www.ncbi.nlm.nih.gov/books
- https://rarediseases.org/rare-diseases
Medical Disclaimer
This information is for educational purposes only. Always consult healthcare professionals for medical advice, diagnosis, and treatment.