Spinocerebellar ataxias represent a large group of rare, progressive neurodegenerative diseases that affect the cerebellum and its connections and predominantly manifest themselves in a cerebellar syndrome. In addition to progressive motor disability, which manifests itself in unsteady gait, limb incoordination or dysarthria, the disease is often accompanied by cerebellar cognitive-affective syndrome. This encompasses a spectrum of cognitive and neuropsychiatric deficits, with impairment of executive, linguistic and visuospatial functions in the foreground.
Autoren
- Dr. Ulf Blanke
Publikation
- InFo NEUROLOGIE & PSYCHIATRIE
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