Wilson's Disease

A rare autosomal recessive (inherited from both parents) disorder of metabolism in which the liver does not excrete the copper in the bile.  This copper accumulates in various tissues in the body, especially the liver, kidneys, brain, and cornea.  Untreated, it can lead to liver damage and brain damage.  Symptoms include tremors, spasticity, and rigidity.  Treatment involves taking the drug penicillamine for life.