Abstract
In this issue of Parkinsonism and Related Disorders (Movements Disorders Round), Wrigley et al. (Reta Lila Weston Institute, UCL, Queen Square Institute of Neurology, London, UK) present an interesting case report of an 18-year-old patient, with an ataxia-dystonia syndrome [1]. Dystonia was the predominant presentation, classified as right hemidystonia (with writer's cramp in the right hand and dystonia in the right foot), associated with mild signs of cerebellar ataxia and with minimal deficit of vibratory sensitivity in the right lower limb [1].
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