Autosomal recessive spinocerebellar ataxia 10
MONDO:0013392Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the ANO10 gene.
Also known as: ANO10 autosomal recessive cerebellar ataxia, SCAR10, autosomal recessive cerebellar ataxia caused by mutation in ANO10, autosomal recessive spinocerebellar ataxia type 10, spinocerebellar ataxia, autosomal recessive type 10, adult-onset autosomal recessive cerebellar ataxia, spinocerebellar ataxia, autosomal recessive 10
18 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive spinocerebellar ataxia 10 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