Spinocerebellar ataxia, autosomal recessive 24
MONDO:0014934Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the UBA5 gene.
Also known as: SCAR24, UBA5 autosomal recessive cerebellar ataxia, autosomal recessive cerebellar ataxia caused by mutation in UBA5, spinocerebellar ataxia, autosomal recessive 24, spinocerebellar ataxia, autosomal recessive 24; SCAR24, spinocerebellar ataxia, autosomal recessive type 24
18 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia, autosomal recessive 24 itself.
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Brain study sheds light on Parkinson's and tics
Knowledge-focused CompletedThis completed study from the National Institute of Neurological Disorders and Stroke aimed to better understand how the brain controls movement and what goes wrong in movement disorders like Parkinson's disease, Tourette's syndrome, and dystonia. Over 1,200 adults—both patients …
Sponsor: National Institute of Neurological Disorders and Stroke (NINDS) • Aim: Knowledge-focused
Last updated Sep 20, 2026 00:00 UTC
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Wrist-Worn gadget could help doctors monitor Parkinson's at home
Knowledge-focused CompletedThis study tested a wrist-worn device called the Personal KinetiGraph (PKG) to see if it can accurately measure movement problems in people with Parkinson's disease. Nineteen participants wore the device while researchers compared its readings to standard clinical tests and video…
Sponsor: Global Kinetics Corporation • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:54 UTC