Striatal degeneration, autosomal dominant 2
MONDO:0014835Any striatal degeneration, autosomal dominant in which the cause of the disease is a mutation in the PDE10A gene.
Also known as: striatal degeneration, autosomal dominant, ADSD2, PDE10A striatal degeneration, autosomal dominant, striatal Degeneration, autosomal dominant 2, striatal Degeneration, autosomal dominant type 2, striatal degeneration, autosomal dominant 2; ADSD2, striatal degeneration, autosomal dominant caused by mutation in PDE10A
12 clinical trials for this condition and its sub-types, 0 tagged with Striatal degeneration, autosomal dominant 2 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