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- W2076514144 abstract "As Wilson's disease is both preventable and treatable, the diagnosis must not be missed. Despite this, it is usually misdiagnosed. Misdiagnosis and delay in treatment are clinically relevant because if left untreated, Wilson's disease progresses to hepatic failure or severe neurologic disability, and death. Those adequately treated have a normal life span. Wilson's disease is an autosomal recessive disease caused by mutations in the ATP7B gene. Mutations in ATP7B result in abnormal copper metabolism and subsequent toxic accumulation of copper. The clinical manifestations of neurologic Wilson's disease include variable combinations of dysarthria, dystonia, tremor, parkinsonism, ataxia, and choreoathetosis. Once the possibility of Wilson's disease is considered, diagnosis is straight forward. Currently available treatments, including zinc acetate and trientine, are generally well tolerated and effective." @default.
- W2076514144 created "2016-06-24" @default.
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- W2076514144 date "2013-05-15" @default.
- W2076514144 modified "2023-09-25" @default.
- W2076514144 title "Recognition and Treatment of Neurologic Wilson's Disease" @default.
- W2076514144 doi "https://doi.org/10.1055/s-0033-1334476" @default.
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