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
People also ask
What is a hepatolenticular degeneration?
What is the life expectancy for people with Wilson's disease?
Can Wilson disease be cured?
What are the mental symptoms of Wilson's disease?
Wilson disease or hepatolenticular degeneration is an autosomal recessive disease which results in an excess copper build up in the body.
Hepatolenticular degeneration is a rare, progressive and fatal disease characterized by extrapyramidal signs, degenerative changes in the basal ganglions,
Jan 13, 2010 · Hepatolenticular degeneration is evidently a very complex disease. A disorder of copper metabolism, resulting in a large positive balance of ...
Hepatolenticular Degeneration: Wilson's Disease · Authors · Affiliations · Box 45-1.
Learn how to diagnose and treat the causes and symptoms of Wilson's disease – or hepatolenticular degeneration – from the team of liver specialists at Bon