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Wil·son's disease

n :  a hereditary disease that is determined by an autosomal recessive gene and is marked esp. by cirrhotic changes in the liver and severe mental disorder due to a ceruloplasmin deficiency and resulting inability to metabolize copper - called also hepatolenticular degeneration  - see KAYSER-FLEISCHER RING 
Wilson, Samuel Alexander Kinnier (1877-1937),
British neurologist. Wilson enjoyed long-term associations with King's College Hospital and the National Hospital for the Paralyzed and Epileptic, both in London. His neurological studies covered such diverse topics as epilepsy, narcolepsy, speech disorders, apraxia, and pathological laughing and crying. In 1912 he published a monograph on progressive lenticular degeneration, which is now known as Wilson's disease. He was the first to detect the relationship between liver disease and putaminous destruction.

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Buchanan General Hospital (Grundy, Virginia - Buchanan County)