Wilson Disease

Wilson Disease

A rare, autosomal recessive disorder characterized by abnormal copper accumulation in the body, particularly in the brain, liver, and cornea.

ATP7B Gene

Mutations in this gene disrupt the transport of copper, leading to its buildup in tissues.

General Symptoms

Tiredness, loss of appetite, jaundice, edema, easy bruising, and prolonged bleeding.

Neurological Symptoms

Speech, swallowing, physical coordination issues, uncontrolled movements, and muscle stiffness.

No Cure

While there is no cure for Wilson disease, it can be managed with proper treatment.

Age Range

Wilson disease can affect a range of ages, from children to adults.

Gender

Both males and females are equally affected by Wilson disease.