Wilson's disease
Also called: hepatolenticular degeneration
An inherited disorder that causes too much copper to accumulate in the organs.
- Treatable by a medical professional
- Requires a medical diagnosis
- Lab tests or imaging always required
- Chronic: can last for years or be lifelong
In Wilson's disease, copper isn't eliminated properly and instead accumulates, possibly to a life-threatening level. Symptoms typically begin between the ages of 12 and 23.
Very rare: Fewer than 20,000 US cases per year
Consult a doctor for medical advice
Sources: Mayo Clinic and others. Learn more
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Wilson disease is a rare genetic disorder passed from parents to children (inherited). It prevents your body from getting rid of extra copper in your system.
What is Wilson disease? Wilson disease (WD) is a rare inherited disorder in which an excessive amount of copper accumulates in the body.
Wilson disease is a rare genetic disorder characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes.
Wilson disease is a rare genetic disorder found in children in which large amounts of copper build up in the liver and brain. Wilson's disease causes liver ...