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Wilson’s Disease: Symptoms and Care

Updated 15 November 20241 min read

What is it?
Wilson’s disease is a rare genetic disorder that prevents the body from eliminating excess copper, leading to copper accumulation in the liver, brain, and other organs.

Symptoms of Wilson’s Disease

  1. Fatigue, jaundice, or swelling (liver-related).
  2. Neurological symptoms like tremors, difficulty speaking, or coordination issues.
  3. Psychiatric symptoms, such as mood changes or depression.

What can I do?

  1. Follow a low-copper diet, avoiding foods like shellfish, nuts, and chocolate.
  2. Take prescribed medications to remove excess copper or prevent absorption.
  3. Attend regular medical check-ups to monitor liver and neurological health.

When to Consult Your Doctor

  • If you experience unexplained liver, neurological, or psychiatric symptoms.
  • If there’s a family history of Wilson’s disease.

Remember
Early diagnosis and treatment of Wilson’s disease can prevent serious complications. Lifelong care and adherence to treatment plans are essential.

This information was created with the help of AI and approved for publication by qualified healthcare providers. It is general information, not a replacement for advice from your doctor, nurse or pharmacist.

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