P57 Adult onset stills disease: clinical features, disease course and outcome in 29 patients
نویسندگان
چکیده
منابع مشابه
A Case of Adult Onset Stills Disease
Adult-onset Still's disease (AOSD) is characterized by fever, rash, and joint pain and may lead to chronic arthritis. The cause of AOSD is unknown, and it is rare. We encountered a patient with adult-onset Still's disease following a sore throat and fever. The patient was a 40-year-old woman who consulted our hospital because of a sore throat, fever and arthritis. She was admitted and treated w...
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Schizophrenia in children is diagnosed by using adult criteria. Based on the age of onset, patients with childhood onset schizophrenia (COS) are subdivided into those with very early onset (before age 12-14 years) and those with early onset (between 14-17 years). The prevalence of COS is reported to be 1 in 10,000 before the age of 12 years; however, there is a significant increase around puber...
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Mazaheri Sh1, Fazlian MM2, Hossein Zadeh A3 1. Assistant Professor, Department of Neurology, Faculty of medicine, Hamedan University of Medical Sciences 2. General practitioner, Specialty and Subspecialty Hospital of Besat, Hamedan University of Medical Sciences 3. General practitioner, Hamedan Health Center Abstract Background: Multiple Sclerosis (MS) is one of the most common causes of chr...
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Kikuchi-Fujimoto disease (KFD) is a rare cause of cervical lymphadenitis which mostly affects Asian women but is sometimes observed in the pediatric population. This study analyzed the clinical manifestations and disease course in children with KFD. Retrospective chart review and telephone interview were used to collect data for 13 children (8 boys and 5 girls) with a diagnosis of KFD from Janu...
متن کاملAdult-Onset Still’s Disease with Parkinsonian Features
Adult-Onset Still’s Disease (AOSD) is a systemic inflammatory rheumatologic disorder characterized by some or all of the following features: fever of unknown origin, an evanescent maculopapular rash, arthritis or arthralgias, pharyngitis, hepatosplenomegaly, lymphadenopathy, and serositis. The pathophysiological basis of AOSD has yet to be described. This rare disease has been associated occasi...
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ژورنال
عنوان ژورنال: Indian Journal of Rheumatology
سال: 2009
ISSN: 0973-3698
DOI: 10.1016/s0973-3698(09)60075-3