Study of genetic causes of spinocerebellar ataxia
Treatments studied
Part of Brain & nervous system, Genetic & congenital clinical trials.
This study follows people with certain types of spinocerebellar ataxia (a group of conditions that cause progressive movement problems) to understand how the disease changes over time and how genes might influence it. It may help researchers learn more about these conditions and support future treatments.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Are age 6 or older and have symptoms of ataxia with a genetic diagnosis of one of the listed SCA types (1, 2, 3, 6, 7, 8, 10, 27B, or RFC1) in yourself or a first-degree relative.
- Or are age 18 or older and have a confirmed genetic diagnosis of one of the listed SCA types.
- Or were a participant in the READISCA study and are willing to join again.
- You must be willing and able to give informed consent to participate.
- For the MRI part: must be 18 or older, have a genetic diagnosis of SCA1, 2, or 3, have a low symptom score (SARA < 10), and be able to have an MRI (not pregnant, no other neurological conditions).
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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