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What is Wilson"s disease?

Wilson"s disease is an inherited condition in which copper is not excreted properly from the body. The excess copper can build up in the liver and/or brain causing liver damage and/or neurological problems. It can also collect in other parts of the body including the eyes and the kidneys.
Copper begins to accumulate immediately after birth but the symptoms usually appear in the 2nd to 3rd decade. The first signs are hepatic (liver) in about 40% of cases, neurological (brain) in about 35% of cases and psychiatric, renal (kidney), haematological (blood), or endocrine (glands) in the remainder.



 
  • What is Wilson"s disease?
  • Metabolic pathway of copper
  • How does this occur?
  • Diagnostic tests for Wilson"s disease
  • History. To whom are we obliged by a life?
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