Autosomal recessive spinocerebellar ataxia 17
MONDO:0014503Any autosomal recessive congenital cerebellar ataxia in which the cause of the disease is a mutation in the CWF19L1 gene.
Also known as: CWF19L1 autosomal recessive congenital cerebellar ataxia, SCAR17, autosomal recessive congenital cerebellar ataxia caused by mutation in CWF19L1, autosomal recessive spinocerebellar ataxia type 17, spinocerebellar ataxia autosomal recessive type 17, spinocerebellar ataxia, autosomal recessive type 17, autosomal recessive cerebellar ataxia due to CWF19L1 deficiency, spinocerebellar ataxia, autosomal recessive 17
18 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive spinocerebellar ataxia 17 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