Still's disease


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Synonyms for Still's disease

a form of rheumatoid arthritis that affects children

References in periodicals archive ?
(TOKYO: 4519) announced today that it has obtained regulatory approval for the humanized anti-human IL-6 receptor monoclonal antibody, "Actemra[R] Intravenous Infusion 80 mg, 200 mg, and 400 mg" (generic name: tocilizumab [genetical recombination]) from the Ministry of Health, Labour and Welfare (MHLW) for an additional indication of "adult Still's disease that has not responded sufficiently to existing therapies" and an additional dosing regimen for the indication.
Many of these diseases, other than PFAPA and adult-onset Still's disease, are associated with genetic mutations.
First described in children by George Still in 1896, "Still's disease" has become the eponymous term for systemic juvenile idiopathic arthritis [4].
Since "The Big Sick" hit theaters and became one of unexpected success stories in film in 2017, Gordon has become something of an advocate for those suffering from Still's disease, often sharing her real-life story with reporters and at conferences -- which Nanjiani said fills him with pride.
Shoenfeld, "The hyperferritinemic syndrome: macrophage activation syndrome, Still's disease, septic shock and catastrophic antiphospholipid syndrome," BMC Medicine, vol.
Bielory, "Diagnosis and management of adult onset Still's disease," Annals of the Rheumatic Diseases, vol.
MAS has been reported in patients with various rheumatic diseases, such as systemic juvenile idiopathic arthritis (sJIA), adult-onset Still's disease, dermatomyositis, and systemic lupus erythematosus (SLE) [1].
She had been put into a medically induced coma after coming down with an extremely rare illness, adult-onset Still's disease. At the time, Nanjiani, a Pakistani-American, was hiding their relationship from his parents, who wanted him to enter into an arranged marriage.
M2 EQUITYBITES-November 16, 2017-Sobi investigates the safety and efficacy of anakinra in patient with Still's disease under phase 3 clinical study
M2 PHARMA-November 16, 2017-Sobi investigates the safety and efficacy of anakinra in patient with Still's disease under phase 3 clinical study
Louis, MO, September 05, 2017 --(PR.com)-- The International Still's Disease Foundation, Inc.
Adult-onset Still's disease (AOSD) is an auto-inflammatory disorder, characterized by spiking fevers, evanescent salmon-pink rash, arthritis or arthralgia, and hyperleukocytosis.
Differential diagnosis should be established with Adult-onset Still's disease, and Cryopyrin-associated periodic syndrome (especially Muckle-Wells syndrome).
A 41-year-old male patient treated with methylprednisolone (64 mg/day) due to Still's disease for three months was admitted to another hospital with the complaints of fever, loss of strength in the right arm and speech impairment.
Adult-onset Still's disease (AOSD) is a rare systemic inflammatory condition with unknown etiology that is characterized by high spiking fever, arthritis, typically salmonpink maculopapular rash, leukocytosis with neutrophilia, and multiple organs' involvement [1].