CSTB-related disease

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Researchers launch major study to track rare epilepsy EPM1 over time

Knowledge-focused Recruiting now

This study is following 200 people with a confirmed genetic diagnosis of EPM1, a rare and progressive epilepsy disorder. Researchers will collect clinical data and biological samples (blood and urine) over time to understand how the disease progresses. The goal is to identify bio…

Matched conditions: CSTB-RELATED DISEASE

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

Last updated Jun 27, 2026 11:03 UTC

CSTB-related disease

Get alerted when new CSTB-related disease trials appear

Researchers launch major study to track rare epilepsy EPM1 over time