Adult-onset Still's disease: Difference between revisions

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==[[Adult-onset Still's disease historical perspective|Historical Perspective]]==
==[[Adult-onset Still's disease historical perspective|Historical Perspective]]==


==[[Adult-onset Still’s disease classification|Classification]]==
==[[Adult-onset Still's disease classification|Classification]]==


==[[Adult-onset Still’s Disease pathophysiology|Pathophysiology]]==
==[[Adult-onset Still’s Disease pathophysiology|Pathophysiology]]==

Revision as of 23:38, 22 April 2018

Adult-onset Still's disease

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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

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Case #1

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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

Case Studies

Case #1