Wilson Disease Treatment in India
Wilson disease causes a build up of copper in the body. It is very rare. Too much copper can be poisonous.
Copper is a mineral we get from food. Our bodies need it in small amounts. 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. This disease is fatal unless it is treated before serious illness develops.
Causes
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.
Risk Factors
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.
Symptoms
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 most commonly appear in people under 40 years old. In children, the symptoms can be present as early as five years of age.
- Symptoms of excess copper in the liver include:
- Jaundice —yellowing of the skin
- Swollen abdomen
- Pain in the abdomen
- Nausea
- Vomiting blood
- Symptoms of excess copper in the brain include:
- Depression
- Anxiety
- Mood swings
- Aggressive or other inappropriate behaviors
- Difficulty speaking and swallowing
- Tremors
- Rigid muscles
- Problems with balance and walking
- Symptoms of excess copper in the eyes include Kayser-Fleischer rings, which are rusty or brown-colored rings around the iris.
Diagnosis
Wilson disease is rare. 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
- Liver biopsy
Images may be taken of your brain. This can be done with MRI.
Genetic Testing
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.
Treatment
The goals of treatment are to:
- Remove the excess copper
- Prevent copper from building up again
- Improve 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
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.
Dietary Changes
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.
Liver Transplant
A liver transplant may be needed if you have severe liver damage. Transplantation may also be needed if you can not tolerate the side effects of medications.
Prevention
Currently, there are no guidelines to prevent Wilson disease.