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Two cases of Wilson’s disease are reported, in which cortico-subcortical lesions of the frontal lobes predominated, with only slight changes in the basal gangliaThe clinical picture of the condition in the 17-year-old female and 21-year-olc male patient was characterized by the presence of the pyramidal syndrome, epileptic seizures and mental changes superimposed on the typical Wilson type of extrapyramidal syndrome. Biochemical studies confirmed the diagnosis oi hepatolenticular degeneration. The Keiser-Fleischer ring was not found in the male patient.
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Operational Program Digital Poland, 2014-2020, Measure 2.3: Digital accessibility and usefulness of public sector information; funds from the European Regional Development Fund and national co-financing from the state budget.