Warning Signs Of Wilson's Disease To Watch For

Wilson's disease is a genetic condition in which the body cannot remove excess copper, causing it to accumulate in the eyes, brain, liver, and other vital organs. Most cases of this disorder are diagnosed when patients are between five and thirty-five years old, and symptoms typically begin during the teenage years. Liver disease is usually the first symptom in patients with Wilson's disease, and neurological and psychiatric symptoms may develop later. To diagnose this condition, doctors can use blood and urine tests to measure the levels of copper in the body, and genetic tests may be performed to check for the specific mutations associated with this illness. A liver biopsy may be completed so the tissue sample can be checked for excess copper, and some patients may need to have an eye exam using a slit-lamp. Chelating agents, including penicillamine and trientine, are typically the first line of treatment for this condition. These medications enable the body to release excess copper through urination, and they must be taken for the patient's entire life. If severe liver damage has occurred as a result of the disease, a liver transplant may be needed. While Wilson's disease is a lifelong condition, early detection means the vast majority of patients lead normal lives.