Treatment & Care
What are the treatments for Wilson’s disease?
Treatment involves medications that promote excretion of copper from your child’s body and prevent it from accumulating again.
Getting rid of the copper
Drugs like penicillamine and trientine work by binding to copper (a process called chelation) and causing it to be excreted through the urine.
Your child will need to take these medications for the rest of his life.
Preventing it from accumulating again
Once the existing copper is removed from the body, taking zinc may help to prevent it from reaccumulating. Zinc helps to block the body's absorption of copper.
Dietary changes may also be recommended in conjunction with medication therapy, including taking vitamin B6 supplements (only if taking penicillamine).
You child’s doctor may also advise avoiding foods high in copper such as the following:
- dried fruit
In advanced stages of liver disease brought on by Wilson's disease, a liver transplant may be necessary.
What is the long-term outlook for patients with Wilson’s disease?
With proper diagnosis and treatment, the progress of Wilson’s disease can be stopped and your child’s symptoms may improve.
It’s important to diagnose and treat Wilson's disease as early as possible. Symptoms of the disease are progressive and, left untreated, may cause irreversible damage.