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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. Anakinra - Wikipedia

    en.wikipedia.org/wiki/Anakinra

    More than ten percent of people taking Anakinra have injection site reactions, headaches, and have increased cholesterol levels. [1] Recipients have eight percent more patients decrease white blood cells counts, two percent more patients decrease platelets counts, one percent more patients get severe infections (4.5% for patients with asthma compared to 0% placebo patients with asthma). [1]

  4. Inflammatory arthritis - Wikipedia

    en.wikipedia.org/wiki/Inflammatory_arthritis

    Inflammatory arthritis is a group of diseases which includes: rheumatoid arthritis, psoriatic arthropathy, inflammatory bowel disease, adult-onset Still's disease, scleroderma, juvenile idiopathic arthritis, and systemic lupus erythematosus (SLE). [1]

  5. 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]

  6. Still's disease - Wikipedia

    en.wikipedia.org/wiki/Still's_Disease

    Adult-onset Still's disease This page was last edited on 29 July 2015, at 09:55 (UTC). Text is available under the Creative Commons Attribution ...

  7. 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 ]

  8. Mysterious new allergies? 6 reasons why adult-onset ... - AOL

    www.aol.com/lifestyle/mysterious-allergies-6...

    These changes are “leading to a rise in new-onset adult allergies,” says Ogden. 2. Hormonal changes and pregnancy ... However, he says that with the right diagnosis and treatment “patients ...

  9. Periodic fever syndrome - Wikipedia

    en.wikipedia.org/wiki/Periodic_fever_syndrome

    Periodic fever syndromes are a set of disorders characterized by recurrent episodes of systemic and organ-specific inflammation.Unlike autoimmune disorders such as systemic lupus erythematosus, in which the disease is caused by abnormalities of the adaptive immune system, people with autoinflammatory diseases do not produce autoantibodies or antigen-specific T or B cells.