New DNA reader may crack the code of mysterious childhood epilepsy
NCT ID NCT07396883
First seen Feb 10, 2026 · Last updated Apr 24, 2026 · Updated 4 times
Summary
This study tests a new DNA-reading technology called long-read genome sequencing in 20 children with severe epilepsy whose standard genetic tests came back normal. The goal is to find hidden genetic errors that current methods miss. If successful, this could lead to better treatments and genetic counseling for families.
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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.
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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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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American Memorial Hospital
Reims, 51092, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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CHU Jean Minjoz
Besançon, 25000, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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CHU de Nancy - hôpital d'enfant
Vandœuvre-lès-Nancy, 54511, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Hôpitaux Universitaires de Strasbourg
Strasbourg, 67098, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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