Wilson's disease: Difference between revisions
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{{CMG}}; '''Associate Editor-In-Chief:''' {{CZ}} | {{CMG}}; '''Associate Editor-In-Chief:''' {{CZ}} | ||
{{SK}} Hepatolenticular degeneration. | |||
== [[Wilson's disease overview|Overview]] == | == [[Wilson's disease overview|Overview]] == | ||
Revision as of 16:30, 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 |
Diagnosis |
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Treatment |
Wilson's disease On the Web |
American Roentgen Ray Society Images of 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
Differential Diagnosis
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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