Age is the main risk factor for adult Still's disease, with incidence in adults peaking twice: once from 15 to 25 years and again from 36 to 46 years. Males and females are equally at risk of acquiring the disorder. Multiple cases of adult Still's disease in families are uncommon, so it's unlikely that this disorder is inherited.
April 03, 2013
- Papadakis MA, et al. Current Medical Diagnosis & Treatment 2013. 52nd ed. New York, N.Y.: The McGraw-Hill Companies; 2013. http://www.accessmedicine.com/resourceTOC.aspx?resourceID=1. Accessed Feb. 8, 2013.
- Mandl LA, et al. Clinical manifestations and diagnosis of adult Still's disease. http://www.uptodate.com/home. Accessed Feb. 8, 2013.
- Mandl LA, et al. Treatment of adult Still's disease. http://www.uptodate.com/home. Accessed Feb. 8, 2013.
- Chang-Miller A (expert opinion). Mayo Clinic, Phoneix/Scottsdale, Ariz. Feb. 15, 2013.
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