Written & medically reviewed by Dr. Sanjay Anbu, MBBS· Last reviewed
Wilson's disease is a rare inherited condition where copper builds up in the body, especially the liver and brain, because the body cannot remove it properly. Early treatment prevents damage.
Medicines that remove copper (chelating agents) or block its absorption (zinc)
A low-copper diet — avoid liver, shellfish, nuts and chocolate
Lifelong treatment and monitoring
Screening of close family members
Liver transplant for severe liver failure
When to see a doctor urgently
Yellow eyes or skin, or unexplained liver problems in a young person
A new tremor, speech or movement changes
Changes in behaviour or mood with liver signs
A family history of the disease
Not a diagnosis. MedDroid gives general educational information about wilson's disease. It cannot examine you, diagnose or prescribe — always confirm with a qualified doctor.
Frequently asked questions
Can Wilson's disease be treated?
Yes. With lifelong copper-lowering treatment and a low-copper diet, most people do very well. Early diagnosis, before organ damage, gives the best outcome.
Is Wilson's disease inherited?
Yes. It is passed on when a child inherits a faulty copper gene from both parents. Siblings of an affected person should be screened.
Reviewed by Dr. Sanjay Anbu, MBBS. MedDroid is an AI medical assistant and can make mistakes. It provides general health information, not a diagnosis or medical advice — always consult a qualified clinician. In an emergency, contact your local emergency number immediately.