Cerebellar ataxia is a form of ataxia originating in the cerebellum. Cerebellar ataxia can occur as a result of many diseases and may present with symptoms of an inability to coordinate balance, gait, extremity and eye movements. To understand the clinical and genetic characteristics of cerebellar ataxia, we establish a registered cohort to follow up Chinese patients with cerebellar ataxia.
Patients with cerebellar ataxia based on the diagnoses of tow neurologists
Relatives of patients with cerebellar ataxia
Unrelated healthy controls
Participants or legal guardian(s) willing and able to complete the informed consent process
Participants are unable to comply with trial procedures and visit schedule
Patients with cerebellar ataxia who are diagnosed by tow neurologists in the Organization in South-East China for Cerebellar Ataxia Research (OSCCAR) from the First Affiliated Hospital of Fujian Medical University.
Cohort
Prospective
No intervention
Other interventionNo intervention
The incidence of hereditary cerebellar ataxia
Look for the causative gene in the patient with cerebellar ataxia
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Ning Wang, MD., PhD.
Lead sponsor
First Affiliated Hospital of Fujian Medical University
Sponsor institution
