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.
Follow this condition to get notified about new trialsBroader categories
-
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 Jul 04, 2026 00:00 UTC
-
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