Wilson's disease: Difference between revisions

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{{SK}} Hepatolenticular degeneration.
{{SK}} Hepatolenticular degeneration.
== [[Wilson's disease overview|Overview]] ==
== [[Wilson's disease overview|Overview]] ==


== [[Wilson's disease historical perspective|Historical Perspective]] ==
== [[Wilson's disease historical perspective|Historical Perspective]] ==
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== [[Wilson's disease pathophysiology|Pathophysiology]] ==
== [[Wilson's disease pathophysiology|Pathophysiology]] ==


== [[Wilson's disease differential diagnosis|Differential Diagnosis]] ==
== [[Wilson's disease differential diagnosis|Differentiating Wilson's disease from other Diseases]] ==
 
 





Revision as of 18:02, 24 August 2012

For patient information click here

Wilson disease
Mutations in the ATP7B gene are present in the majority of patients with Wilson's disease.
ICD-10 E83.0
ICD-9 275.1
OMIM 277900
DiseasesDB 14152
MedlinePlus 000785
MeSH D006527

Wilson's disease Microchapters

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Risk calculators and risk factors for Wilson's disease

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]

Synonyms and keywords: Hepatolenticular degeneration.

Overview

Historical Perspective

Pathophysiology

Differentiating Wilson's disease from other Diseases

Epidemiology and Demographics

Diagnosis

History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | CT | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies

Treatment

Medical therapy | Surgery | Cost-effectiveness of Therapy | Future or Investigational Therapies Template:Mineral metabolic pathology

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