Cognition and psychopathology in myoclonus-dystonia
Journal of Neurology, Neurosurgery & Psychiatry, 06/12/2012
van Tricht MJ et al. – The findings of this study suggest that anxiety disorders and executive dysfunctions may be part of the phenotype of myoclonus–dystonia (M–D) patients with a DYT11 mutation, whereas depressive symptoms and semantic fluency impairments may be secondary to suffering from a chronic movement disorder, regardless of DYT11 gene mutation.
