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Epileptic encephalopathy, childhood-onset

Clinical trials for Epileptic encephalopathy, childhood-onset explained in plain language.

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Can mapping a rare Gene's effects pave the way to targeted epilepsy therapies?

Knowledge-focused Ongoing

This study follows children aged 6 to 21 who have a CNKSR2 gene mutation, which can cause epilepsy, language difficulties, and intellectual disability. Researchers will use brain scans, EEGs, and developmental tests to track how the condition changes over time. The goal is to cre…

Matched conditions: EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET

Sponsor: University of California, San Francisco • Aim: Knowledge-focused

Last updated Jul 25, 2026 00:00 UTC

Epileptic encephalopathy, childhood-onset

Get alerted when new Epileptic encephalopathy, childhood-onset trials appear

Can mapping a rare Gene's effects pave the way to targeted epilepsy therapies?