Autosomal recessive ataxia, Beauce type
MONDO:0012549A rare disorder characterized by a slowly progressive pure cerebellar ataxia associated with dysarthria. It has been described in 53 individuals from 26 families of Canadian origin. The mode of transmission is autosomal recessive. Positional cloning has led to the identification of several gene mutations.
Also known as: ARCA1, SCAR8, autosomal recessive cerebellar ataxia type 1, spinocerebellar ataxia, autosomal recessive type 8, SYNE1-related autosomal recessive cerebellar ataxia, ataxia, recessive, of Beauce, autosomal recessive ataxia Beauce type, autosomal recessive spinocerebellar ataxia 8
18 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive ataxia, Beauce type itself.
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Robots as rehab coaches: a new approach to retraining coordination in ataxia
Disease control OngoingThis trial tests whether robot-assisted neurorehabilitation can improve coordination, balance, and walking in adults with ataxia, a condition that affects movement control. Participants will receive either robotic or standard rehabilitation, and researchers will measure changes i…
Sponsor: Somogy Megyei Kaposi Mór Teaching Hospital • Aim: Disease control
Last updated Jul 31, 2026 00:00 UTC
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Can a gentle brain zap help people with ataxia walk better?
Symptom relief OngoingThis study tests whether a non-invasive brain stimulation technique called transcranial direct current stimulation (tDCS) can improve movement in people with degenerative ataxia, a rare condition that damages the cerebellum and impairs balance and coordination. Sixteen participan…
Sponsor: University of Cagliari • Aim: Symptom relief
Last updated Jun 27, 2026 08:00 UTC