MYOCLONUS EPILEPSIES, PROGRESSIVE

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Scientists launch national registry to map devastating rare epilepsy

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This study aims to understand how a rare, severe genetic epilepsy called EPM1 progresses over time. Researchers will remotely track symptoms and collect blood and urine samples from up to 200 participants across the US who have a confirmed genetic diagnosis. The goal is to gather…

Matched conditions: MYOCLONUS EPILEPSIES, PROGRESSIVE

Sponsor: Boston Children's Hospital • Aim: Knowledge-focused

Last updated Apr 01, 2026 14:43 UTC

MYOCLONUS EPILEPSIES, PROGRESSIVE

Get alerted when new MYOCLONUS EPILEPSIES, PROGRESSIVE trials appear

Scientists launch national registry to map devastating rare epilepsy