Autosomal recessive spinocerebellar ataxia 11
MONDO:0013645Any autosomal recessive syndromic cerebellar ataxia in which the cause of the disease is a mutation in the SYT14 gene.
Also known as: SCAR11, SYT14 autosomal recessive syndromic cerebellar ataxia, autosomal recessive spinocerebellar ataxia 11, autosomal recessive spinocerebellar ataxia type 11, autosomal recessive syndromic cerebellar ataxia caused by mutation in SYT14, spinocerebellar ataxia, autosomal recessive type 11, autosomal recessive cerebellar ataxia-psychomotor retardation syndrome, spinocerebellar ataxia, autosomal recessive 11
18 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive spinocerebellar ataxia 11 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