NL-OMON34216
Recruiting
N/A
Cerebellar dysfunction and its compensation in presymptomatic carriers of dominant ataxia genes - Cerebellar changes in presymptomatic SCA-carriers
niversitair Medisch Centrum Sint Radboud0 sites50 target enrollmentTBD
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Cerebellar ataxia
- Sponsor
- niversitair Medisch Centrum Sint Radboud
- Enrollment
- 50
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Proven mutation in one of the SCA genes
- •Age \> 18 years
- •Free of ataxia
Exclusion Criteria
- •Contraindications for MRI scanning (e.g. pacemaker)
- •Other neurological disorders
- •Gait disorder for any reason
Outcomes
Primary Outcomes
Not specified
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