Genotype-phenotype Correlation and Pathogenic Mechanism in Hereditary Ataxia
Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY
The investigators aimed to find appropriate biomarkers such as serum neurofilament light chain in reflecting disease severity in hereditary ataxia from a large cohort during long-term follow-up. The disease severity is indicated by clinical scales and brain MRI tests.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:
• genetically diagnosed as Spinocerebellar ataxia
Locations
Other Locations
China
Second Affiliated Hospital, Zhejiang University School of Medicine
RECRUITING
Hangzhou
Contact Information
Primary
Yi Dong
dongyi720@zju.edu.cn
+ 8618367129345
Time Frame
Start Date: 2021-06-30
Estimated Completion Date: 2025-12-25
Participants
Target number of participants: 500
Related Therapeutic Areas
Sponsors
Leads: Second Affiliated Hospital, School of Medicine, Zhejiang University