Gene-Sequencing breakthrough could unlock mysteries of childhood epilepsy
NCT ID NCT03652246
First seen Mar 22, 2026 · Last updated May 24, 2026 · Updated 12 times
Summary
This study tested a new genetic test (exome sequencing) to find the cause of severe epilepsy with developmental delays in 15 children whose standard tests were normal. The goal was to see if this advanced approach could identify more genetic causes, helping families get clearer answers and better genetic counseling. The study focused on children with suspected inherited forms of the condition.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Chu Dijon Bourogne
Dijon, 21000, France
Conditions
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