Signs and Symptoms
People with Wilson disease who have liver involvement typically develop symptoms starting in early childhood; those with brain involvement may have neurologic and psychiatric symptoms beginning in their teens or early twenties, but the age range for both can vary from about three years old to more than fifty.
People with brain involvement may have a range of physical symptoms, including:
- Siff face muscles
- Abnormal eye movements
- Altered gait
- Difficulty walking, speaking, and swallowing
They may also experience behavioral changes such as depression, paranoia, impulsiveness, obsessive behavior, aggression, and a shortened attention span.
About 50% of those with liver disease and 90% of those with brain involvement will have Kayser-Fleischer rings, deposits of copper in a ring around the cornea that can be seen with an eye exam called a slit lamp examination.
Some with Wilson disease may also experience anemia, easy bruising, joint pain, and/or kidney dysfunction.
Left untreated, Wilson disease tends to become progressively worse and is eventually fatal. With early detection and treatment, most of those affected can live relatively normal lives. Liver and neurologic damage that occurs prior to treatment may improve, but it is often permanent.