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.
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* 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
Exclusion Criteria:
* Participants are unable to comply with trial procedures and visit schedule
Primary outcome measure(s)
The incidence of hereditary cerebellar ataxia — Up to 20years Look for the causative gene in the patient with cerebellar ataxia
Trial sites (1)
Facility
City
Region
Status
Department of Neurology ,First Affiliated Hospital Fujian Medical University
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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