Hunting for hidden genetic triggers of severe childhood epilepsy

NCT ID NCT02890641

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aims to find genetic mutations in the brain that cause drug-resistant epilepsy in children. Researchers will compare DNA from blood and brain tissue, including samples from special electrodes placed in the brain. The goal is to better understand the root causes of these severe seizures, not to test a new treatment.

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Conditions

The condition(s) this trial relates to.

congenital hypothalamic hamartoma syndrome encephalitis Focal Cortical Dysplasia focal epilepsy glioma hemimegalencephaly isolated focal cortical dysplasia Rasmussen subacute encephalitis Sturge-Weber syndrome tuberous sclerosis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Fondation Ophtalmologique Adolphe de Rothschld

    RECRUITING

    Paris, 75019, France

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact