The treatment of Wilson’s disease, a rare genetic disorder of copper metabolism

Purchase, Rupert (2013) The treatment of Wilson’s disease, a rare genetic disorder of copper metabolism. Science Progress, 96 (1). pp. 19-32. ISSN 0036-8504

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Abstract

Wilson’s disease is a rare autosomal recessive disease characterised by the deposition of copper in the brain, liver, cornea, and other organs. The overload of copper inevitably leads to progressive liver and neurological dysfunction. Copper overload in patients with Wilson’s disease is caused by impairment to the biliary route for excretion of dietary copper. A combination of neurological (particularly psychiatric) and hepatic symptoms can make the diagnosis of Wilson’s disease challenging. Most symptoms appear in the second and third decades of life. The disease affects between one in 30,000 and one in 100,000 individuals, and is fatal if left untreated. Five drugs are currently available to treat Wilson’s disease: British Anti-Lewisite; D-penicillamine; trientine; zinc sulfate or acetate; and ammonium tetrathiomolybdate. Each drug can reduce copper levels and/or transform copper into a metabolically inert and unavailable form in the patient. The discovery and introduction of these five drugs owes more to the inspiration of a few dedicated physicians and agricultural scientists than to the resources of the pharmaceutical industry.

Item Type: Article
Keywords: Hepatolenticular degeneration, Wilson’s disease, copper metabolism, British Anti-Lewisite, D-penicillamine, trientine, zinc, ammonium tetrathiomolybdate
Schools and Departments: School of Life Sciences > Chemistry
Depositing User: Rupert Purchase
Date Deposited: 11 Dec 2017 13:48
Last Modified: 11 Dec 2017 13:48
URI: http://sro.sussex.ac.uk/id/eprint/71964

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