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Adult-onset Still's disease is rare and has been described all over the world. The number of new cases per year is estimated to be 1.6 per 1,000,000 population. [ 1 ] The number of people currently affected is estimated at 1.5 cases per 100,000–1,000,000 population. [ 22 ]
Systemic-onset juvenile idiopathic arthritis (sJIA), also known as Still disease, Still's disease, and systemic juvenile idiopathic arthritis, is a subtype of juvenile idiopathic arthritis (JIA) that is distinguished by arthritis, a characteristic erythematous skin rash, and remitting fever. [5]
UN: Estimate of life expectancy for various ages in 2023; Locations Life expectancy for population in general Life expectancy for male Life expectancy for female Sex gap; at birth bonus 0→15 at 15 bonus 15→65 at 65 bonus 65→80 at 80 at birth at 15 at 65 at 80 at birth at 15 at 65 at 80 at birth at 15 at 65 at 80 Hong Kong: 85.51: 0.21: 70 ...
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The life expectancy in some states has fallen in recent years; for example, Maine's life expectancy in 2010 was 79.1 years, and in 2018 it was 78.7 years. The Washington Post noted in November 2018 that overall life expectancy in the United States was declining although in 2018 life expectancy had a slight increase of 0.1 and bringing it to ...
Usual onset: Adulthood: Duration: Lifelong: Causes: Genetic mutation: Diagnostic method: Genetic testing: Differential diagnosis: Multiple sclerosis: Prevention: none: Prognosis: Bad, but quality of life can be improved with treatment: Frequency: rare, at least 70 people on Earth have been diagnosed with the condition: Deaths: Inevitable in ...
After the gap between male and female life expectancy widened in 2021, overall male life expectancy improved by 1.3 years while life expectancy for women improved 0.9 years. Females were still ...
In addition, MAS has been described in association with systemic lupus erythematosus (SLE), Kawasaki disease, and adult-onset Still's disease. It is thought to be closely related and pathophysiologically very similar to reactive (secondary) hemophagocytic lymphohistiocytosis (HLH). [ 1 ]