Adult-onset Still's disease: Difference between revisions
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{{SK}} Wissler-Fanconi syndrome, AOSD | {{SK}} Wissler-Fanconi syndrome, AOSD | ||
==[[Adult-onset | ==[[Adult-onset Still's disease overview|Overview]]== | ||
==[[Adult-onset Still’s disease Historical perspective|Historical Perspective]]== | ==[[Adult-onset Still’s disease Historical perspective|Historical Perspective]]== |
Revision as of 23:37, 22 April 2018
Adult-onset Still's disease |
Differentiating Adult-onset Still’s Disease from other Diseases |
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Diagnosis |
Treatment |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Synonyms and keywords: Wissler-Fanconi syndrome, AOSD
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Adult-onset Still’s Disease from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic study of choice | History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | X-Ray Findings | Echocardiography and Ultrasound | CT-Scan Findings | MRI Findings | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies