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Article in English | IMSEAR | ID: sea-65618

ABSTRACT

Penicillamine is the standard therapy for Wilson's disease in children. We report an 8-year-old-girl with liver disease due to Wilson's disease who developed extrapyramidal symptoms following administration of penicillamine. Symptoms resolved within 20 hours of stopping the drug but recurred within 24 hours when gradually increasing small doses were recommenced.


Subject(s)
Chelating Agents/adverse effects , Child , Dose-Response Relationship, Drug , Female , Hepatolenticular Degeneration/drug therapy , Humans , Neurodegenerative Diseases/chemically induced , Penicillamine/adverse effects , Syndrome
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