U.S., Aug. 2 -- ClinicalTrials.gov registry received information related to the study (NCT07099651) titled 'Autosomal Dominant Spinocerebellar Ataxias and Social Cognition' on July 17.
Brief Summary: Spinocerebellar ataxias are a group of rare neurodegenerative diseases, clinically and genetically highly heterogeneous, with an estimated mean prevalence of 2.7 per 100,000 population. The term "spinocerebellar ataxia" or "SCA" is often used for ataxias of genetic origin of autosomal dominant transmission, which are the subject of this study. Recent studies of social cognition in patients with genetic cerebellar pathologies, and autosomal dominant spinocerebellar ataxia in particular, are still few and far between (around 15 studies), and see...