Wilson disease causes a buildup of copper in the body. It is very rare.
Copper is a mineral we get from food. Our bodies need it in small amounts. Too much copper can be poisonous.
We eat much more copper than we need. The copper needs to be passed out of our bodies. People with Wilson disease cannot pass the copper they do not need. The copper builds up in the body and damages organs like the liver, brain, kidneys, and eyes.
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Wilson disease is a genetic disorder. A faulty gene causes this system to malfunction. Both parents must have the faulty gene in order for the child to develop the disease. People with only one faulty gene may never have symptoms. However, they can pass the gene on to their children.
The only known factor that increases your risk for Wilson disease is a family history of the disease.
It tends to be most common in eastern Europeans, Sicilians, and southern Italians.
It may take some time for copper to build up. At first, the liver will hold the excess copper. Eventually, the liver will not be able to hold the copper. Copper will begin to leave the liver and move to other organs like the brain or eyes. Symptoms usually begin under 40 years of age, typically at ages 6-20 years. They can be present as early as 5 years of age.
Symptoms of excess copper in the liver include:
Jaundice—yellowing of the skin
and eyesSwollen abdomenPain in the abdomenNauseaVomiting bloodFluid buildup in the legsFatigue
Symptoms of excess copper in the brain include:
DepressionAnxietyMood swingsAggressive or other inappropriate behaviorsDifficulty speaking and swallowingTremorsRigid musclesProblems with balance and walkingSymptoms of excess copper in the eyes include Kayser-Fleischer rings, which are rusty or brown-colored rings around the iris.Symptoms may also occur due to anemia, infections, poor blood clotting, kidney damage, or bone and joint disease from the extra copper
Wilson disease is rare. It is fatal unless it is treated before serious illness develops. Symptoms may be attributed to other more common causes like hepatitis or cirrhosis. You may also appear healthy even while your liver is getting damaged. However, it is important to get diagnosed and treated early. This will help to avoid organ damage and early death.
Your doctor will ask about your symptoms and medical history. A physical and mental exam will be done. Your eyes will be examined for brown, ring-shaped color in the cornea (Kayser-Fleischer rings).
Your bodily fluids and tissues may be tested for copper. This can be done with: Blood and urine tests
Images may be taken of your brain. This can be done with an MRI scan.
You may consider genetic testing if there is a family history of Wilson disease. If the condition is identified before symptoms develop, it may prevent serious complications.
It may also be recommended in people who don't have a history of high alcohol intake but have a fatty liver.
Genetic counseling may be helpful to review risks of genetic testing.
The goals of treatment are to: Remove the excess copperPrevent copper from building up againImprove all associated symptoms of copper overload
Treatment cannot cure the underlying problem of copper build up. You will need to continue treatment throughout your lifetime.
Medications may help by: Binding to the cooper. This helps release copper from organs into blood. Most of the copper will then be filtered in the kidneys and passed in the urine.Blocking the absorption of copper in the digestive tract.
Certain changes in your diet may help reduce your copper intake: Avoid foods high in copper such as liver, shellfish, nuts, chocolate, and mushrooms.Have your drinking water checked for copper levels.Avoid multivitamins with copper.
A liver transplant may be needed if you have severe liver damage. Transplantation may also be needed if you cannot tolerate the side effects of medications.
There are no current guidelines to prevent Wilson disease.
About Wilson disease. Wilson Disease Association website. Available at:
http://www.wilsonsdisease.org/about-wilsondisease.php. Accessed April 26, 2013.
Brewer GJ, Askari F, et al.
Treatment of Wilson disease with ammonium tetrathiomolybdate: IV. Comparison of tetrathiomolybdate and trientine in a double-blind study of treatment of the neurologic presentation of Wilson disease.
Arch Neurol. 2006;63(4):521-527.
Ferenci P. Wilson disease.
Clin Gastroenterol Hepatol. 2005;3(8):726-733.
Wilson disease. EBSCO DynaMed website. Available at:
http://www.ebscohost.com/dynamed. Updated April 8, 2013. Accessed February 27, 2014.
Wilson disease. National Digestive Disease Information Clearinghouse website. Available at:
http://www.niddk.nih.gov/health-information/health-topics/digestive-diseases/wilson-disease/Pages/facts.aspx. Updated April 30, 2012. Accessed April 26, 2013.
Last reviewed February 2015 by Michael Woods, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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