Adult-onset Still's disease epidemiology and demographics: Difference between revisions
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==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
=== | ===Incidence and prevalence=== | ||
* There is a dearth of data regarding the incidence and prevalence of adult-onset Still's disease (AOSD). | |||
=== | * | ||
* In France, the annual incidence of ASD was estimated to be 0.16 per 100,000 individuals.<ref name="pmid7668903">{{cite journal |vauthors=Magadur-Joly G, Billaud E, Barrier JH, Pennec YL, Masson C, Renou P, Prost A |title=Epidemiology of adult Still's disease: estimate of the incidence by a retrospective study in west France |journal=Ann. Rheum. Dis. |volume=54 |issue=7 |pages=587–90 |date=July 1995 |pmid=7668903 |pmc=1009940 |doi= |url=}}</ref> | |||
===Age=== | ===Age=== |
Revision as of 16:22, 20 April 2018
Adult-onset Still's disease |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Epidemiology and Demographics
Incidence and prevalence
- There is a dearth of data regarding the incidence and prevalence of adult-onset Still's disease (AOSD).
- In France, the annual incidence of ASD was estimated to be 0.16 per 100,000 individuals.[1]
Age
- Aging adults affected by adult-onset Still's disease (AOSD) have a higher rate of development of complications related to AOSD and a higher mortality rate compared to younger individuals.
Gender
- Adult-onset Still's disease (AOSD) affects females more than females.
Race
- Adult-onset Still's disease (AOSD) affects Caucasians more than other races.