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  2. Adult-onset Still's disease - Wikipedia

    en.wikipedia.org/wiki/Adult-onset_Still's_disease

    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 ]

  3. Systemic-onset juvenile idiopathic arthritis - Wikipedia

    en.wikipedia.org/wiki/Systemic-onset_juvenile...

    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]

  4. Chronic recurrent multifocal osteomyelitis - Wikipedia

    en.wikipedia.org/wiki/Chronic_recurrent_multi...

    Chronic recurrent multifocal osteomyelitis (CRMO) is a rare condition (1:1,000,000), in which the bones have lesions, inflammation, and pain.It is called multifocal because it can appear in different parts of the body, primarily bones, and osteomyelitis because it is very similar to that disease, although CRMO appears to be without any infection.

  5. Spinal muscular atrophy - Wikipedia

    en.wikipedia.org/wiki/Spinal_muscular_atrophy

    The disease progresses slowly, and most people with SMA 3 lose walking ability sometime in their lives, requiring mobility support. Respiratory involvement is rare and life expectancy is normal or near-normal. 253400: SMA 4 (Adult onset) Adulthood This denotes the adult-onset form, sometimes also classified as a late-onset SMA type 3.

  6. Macrophage activation syndrome - Wikipedia

    en.wikipedia.org/wiki/Macrophage_activation_syndrome

    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 ]

  7. Myotonic dystrophy - Wikipedia

    en.wikipedia.org/wiki/Myotonic_dystrophy

    Life expectancy in non-congenital late-onset or adult onset DM1 is in the early 50s, [5] with pulmonary complications being the leading cause of death, followed by cardiac complications. [27] DM2 life expectancy has yet to be studied.

  8. List of countries by life expectancy - Wikipedia

    en.wikipedia.org/wiki/List_of_countries_by_life...

    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 ...

  9. Autosomal dominant leukodystrophy with autonomic disease

    en.wikipedia.org/wiki/Autosomal_dominant_leuko...

    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 ...