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- W4366721988 abstract "A 72-year-old woman developed progressive choreic movements involving the right hemibody and the orofacial muscles (video 1). Her examination was otherwise unremarkable, without ataxia. Brain MRI, blood glucose, thyroid function, and rheumatologic panel were unremarkable. Genetic testing for Huntington disease and C9orf72 expansions were negative. Initial hematocrit and hemoglobin levels were normal, but increased to abnormal values (56% and 18.5 g/dL) 1 year after chorea onset. The JAK2V617F mutation was positive, suggesting a diagnosis of chorea due to polycythemia vera. Chorea disappeared with phlebotomy and hydroxyurea. Neurologists should suspect this rare treatable entity in elderly patients with chorea even with initially normal hematocrit levels.1" @default.
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- W4366721988 date "2023-04-18" @default.
- W4366721988 modified "2023-10-07" @default.
- W4366721988 title "Teaching Video NeuroImages: A treatable rare cause of chorea" @default.
- W4366721988 cites W2050044815 @default.
- W4366721988 doi "https://doi.org/10.1212/wnl.0000000000206991" @default.
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