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Wilson's disease

   Also found in: Medical, Legal, Encyclopedia, Wikipedia 0.01 sec.
Wil·son's disease  (wlsnz)
n.
A rare hereditary disease caused by a defect in the body's ability to metabolize copper that results in an accumulation of copper deposits in organs such as the brain, liver, and kidneys.

[After Samuel Alexander Kinnier Wilson (1877-1937), British neurologist.]
ThesaurusLegend:  Synonyms Related Words Antonyms
Noun1.Wilson's disease - a rare inherited disorder of copper metabolismWilson's disease - a rare inherited disorder of copper metabolism; copper accumulates in the liver and then in the red blood cells and brain


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The reduced concentration of CP can be a good indicator of Wilson's Disease, where copper is deposited in the skin, liver and brain, resulting in hepatic cirrhosis and neurologic damage.
They cover those associated with Parkinson's disease, chorea, tremor, ataxic syndromes, Huntington's disease, multiple system atrophy, Wilson's disease, and dystonia, for example.
 
 
 
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