Hereditary hyperekplexia
MONDO:0021022Hereditary hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses.
Also known as: hyperekplexia, Kok disease, Stiff baby syndrome, congenital stiff man syndrome, familial startle disease, hereditary hyperekplexia, hereditary hyperexplexia, hyperexplexia hereditary
12 clinical trials for this condition and its sub-types, 0 tagged with Hereditary hyperekplexia itself.
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Sub-types of Hereditary hyperekplexia
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Hyperekplexia 1 0 trials
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Hyperekplexia 2 0 trials
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Hyperekplexia 3 0 trials
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Hyperekplexia 4 0 trials
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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