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Progressive Myoclonic Encephalopathies Due to of Unverricht-Lundborg Disease

Legend: A 17-year-old girl with EPM1 gene mutation, with prominent resting and action myoclonus in the upper and lower limbs causing marked impairment in ambulation.

Duration: 1:18

Associated with: CONTINUUM: Lifelong Learning in Neurology. 19(5):1264-1286, October 2013