Wilson's disease
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| 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 |
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Wilson's disease Microchapters |
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Blogs on Wilson's disease</small> |
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
Mineral metabolic pathology (E83, 275) | |
|---|---|
| Mineral | Cu Wilson's disease/Menkes disease
Fe Haemochromatosis, Aceruloplasminemia, Atransferrinemia Zn Acrodermatitis enteropathica PO43− Hypophosphatemia/Hypophosphatasia Mg2+ Hypermagnesemia/Hypomagnesemia Ca2+ Hypercalcaemia/Hypocalcaemia/Disorders of calcium metabolism Biotin Biotinidase deficiency, Holocarboxylase synthetase deficiency |
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