Wilson Disease is a rare genetic liver disorder where the body retains excess copper. It affects about 1 in 30,000 people worldwide and both parents must carry the gene to pass it on. Symptoms can include issues with speech, swallowing, or mood changes. While it can be deadly, treatments like penicillamine or zinc can help remove excess copper, though the patient requires lifelong treatment to manage the disease.

1. Wilson Disease: A Rare
Liver Disorder
Dr. Lewis Teperman

2. Wilson Disease: A Rare Liver Disorder
 During his more than 30 years with NYU Langone Medical Center, director
of transplant surgery Dr. Lewis Teperman has helped to diagnose a number
of rare liver disorders. One of the rarest liver disorders Dr. Lewis Teperman
has diagnosed is Wilson disease.

3. Wilson Disease: A Rare Liver Disorder
 A condition where the body retains excess copper, Wilson disease affects
about one in 30,000 people worldwide. Both parents must carry the gene to
pass the disease to their children. Copper build-up caused by the disease is
eventually released into the bloodstream and can cause damage in the
brain, eyes, and kidneys, in addition to the liver.

4. Wilson Disease: A Rare Liver Disorder
 Symptoms of the disease can include slurred speech, difficulty swallowing,
or depression and manic behavior, among others. Although it can be
deadly, there are a number of treatments available to patients.
Decoppering agents like penicillamine or high-dose zinc can remove the
toxic concentration of copper, but these substances do not cure the
disease. Treatment must continue throughout the patient’s life to avoid a
life-threatening situation.