Long-read gene testing for inherited movement disorders
Part of Brain & nervous system clinical trials.
This study uses a new DNA reading method to find hidden genetic causes of dystonia. It is for people with dystonia who had standard genetic testing that did not find a cause.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have dystonia that started before age 50 or runs in your family.
- You have already had standard genome sequencing (DNA testing) that did not find a cause.
- You and at least two relatives (affected or unaffected) are able to give a blood sample.
- You are willing to sign an informed consent form.
- Your dystonia is not due to a known non-genetic cause like birth injury or head trauma.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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