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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 (AOSD) is a form of Still's disease, a rare systemic autoinflammatory disease characterized by the classic triad of fevers, joint pain, and a distinctive salmon-colored bumpy rash. The disease is considered a diagnosis of exclusion. [1] Levels of the iron-binding protein ferritin may be extremely elevated with this ...

  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. 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 ]

  5. Still's disease - Wikipedia

    en.wikipedia.org/wiki/Still's_Disease

    Still's disease can refer to: Systemic-onset juvenile idiopathic arthritis; Adult-onset Still's disease This page was last edited on 29 ...

  6. Hemophagocytic lymphohistiocytosis - Wikipedia

    en.wikipedia.org/wiki/Hemophagocytic_lymphohist...

    In rheumatic diseases, this syndrome is more often referred to as macrophage activation syndrome (MAS) and occurs most frequently in the juvenile onset and adult onset forms of Still's disease and in systemic lupus erythematosus. It occurs rarely in juvenile idiopathic arthritis, juvenile Kawasaki disease, and rheumatoid arthritis. [7]

  7. Periodic fever syndrome - Wikipedia

    en.wikipedia.org/wiki/Periodic_fever_syndrome

    Other autoinflammatory diseases that do not have clear genetic causes include adult-onset Still's disease, systemic-onset juvenile idiopathic arthritis, Schnitzler syndrome, and chronic recurrent multifocal osteomyelitis. It is likely that these diseases are multifactorial, with genes that make people susceptible to these diseases, but they ...

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  9. Spondyloarthritis - Wikipedia

    en.wikipedia.org/wiki/Spondyloarthritis

    Criteria for the early diagnosis of axial spondyloarthritis have been developed in light of the emergence of effective treatments. These criteria consider the added value of HLA-B27 testing, as well as current advancements in MRI scanning. [6] [26] Magnetic resonance images of sacroiliac joints: psoriatic arthritis. Shown are T1-weighted semi ...