Status:
RECRUITING
Human Epilepsy Genetics--Neuronal Migration Disorders Study
Lead Sponsor:
Harvard University Faculty of Medicine
Collaborating Sponsors:
National Institute of Neurological Disorders and Stroke (NINDS)
Howard Hughes Medical Institute
Conditions:
Brain Malformation
Neuronal Migration Disorder
Eligibility:
All Genders
Brief Summary
The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.
Detailed Description
Epilepsy is responsible for tremendous long-term healthcare costs. Analysis of inherited epilepsy conditions has allowed for identification of several key genes active in the developing brain. Althoug...
Eligibility Criteria
INCLUSION:
- Males and females of any age.
- Persons with a brain malformation or disorder of cognition (familial intellectual disability [previously known as mental retardation] or autism).
EXCLUSION:
- Persons without a brain malformation or disorder of cognition (familial intellectual disability (previously known as mental retardation] or autism).
Key Trial Info
Start Date :
April 1 1996
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
June 1 2030
Estimated Enrollment :
3500 Patients enrolled
Trial Details
Trial ID
NCT00041600
Start Date
April 1 1996
End Date
June 1 2030
Last Update
September 21 2023
Active Locations (1)
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1
Boston Children's Hospital, Walsh Laboratory
Boston, Massachusetts, United States, 02115