NCT04106765
Unknown
N/A
Clinical, EEG and Radiological Initial and Evolutive Characterisation of LGI1-antibody Patients
ConditionsAnti-LGI1 Encephalitis
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Anti-LGI1 Encephalitis
- Sponsor
- Hospices Civils de Lyon
- Enrollment
- 192
- Locations
- 1
- Primary Endpoint
- Evolution of epileptic seizures
- Last Updated
- 6 years ago
Overview
Brief Summary
Autoimmune encephalitis involve autoantibodies targeting central nervous system, and particularly the synapse or its structure like for LGI1 protein. Anti-LGI1 encephalitis is revealed by an inflammation of the limbic system, with mainly temporal lobe, faciobrachial dystonic or generalized seizures, and cognitive disorders.
This disease is rare and its clinical, EEG and radiological characterisation is not sufficiently established. The investigators will evaluate these three aspects for the anti-LGI1 cohort of patients of the National Reference Center of autoimmune encephalitis.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age \> 18 years
- •Diagnosis of anti-LGI1 encephalitis based on sera or CSF samples in the National Reference Center of autoimmune encephalitis from 2011/06 to 2019 july 1st.
- •Clinical follow-up in France
Exclusion Criteria
- •Anti-LGI1 antibody associated with another encephalitis antibody
- •Foreign follow-up
Outcomes
Primary Outcomes
Evolution of epileptic seizures
Time Frame: 12 MONTHS
Study Sites (1)
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