Wilson's Disease
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Wilson's disease is a rare inherited disorder that causes too much copper to accumulate in your liver, brain and other vital organs. Symptoms typically begin between the ages of 12 and 23. Copper plays a key role in the development of healthy nerves, bones, collagen and the skin pigment melanin. Normally, copper is absorbed from your food, and any excess is excreted through bile — a substance produced in your liver. But in people with Wilson's disease, copper isn't eliminated properly and instead accumulates, possibly to a life-threatening level. When diagnosed early, Wilson's disease is treatable, and many people with the disorder live normal lives.
This video in 30 seconds
This video explains Wilson's disease, a rare inherited disorder in which copper accumulates in the liver, brain and other vital organs. It describes the normal role of copper in the body and how its elimination through bile fails in this disorder.
Key points
- Defines Wilson's disease as a rare inherited disorder causing excess copper accumulation
- Notes symptoms typically begin between the ages of 12 and 23
- Describes copper's role in nerves, bones, collagen and the skin pigment melanin
- Explains that excess copper is normally excreted through bile, but is not eliminated properly in Wilson's disease
Video Overview
This video presents “Wilson's Disease” — Wilson's disease is a rare inherited disorder that causes too much copper to accumulate in your liver, brain and other vital organs. Symptoms typically begin between the ages of 12 and 23. Copper plays a key role in the development of. Whether you are preparing for a procedure, studying the technique, or learning how a condition is assessed, the recording shows the process as it is performed in practice.
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Educational content only — not a substitute for professional medical advice.
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