Wilson's disease

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
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Wilson'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
CT
MRI
Echocardiography or Ultrasound
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Wilson's disease On the Web
Most recent articles
cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Wilson's disease All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Wilson's disease
CDC on Wilson's disease
Wilson's disease in the news
Blogs on Wilson's disease
Directions to Hospitals Treating Wilson's disease
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.

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