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Seizures, benign familial neonatal, 2

MONDO:0007366

Any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ3 gene.

Also known as: KCNQ3 benign neonatal seizures, benign neonatal seizures caused by mutation in KCNQ3, seizures, benign familial neonatal, 2, seizures, benign familial neonatal, type 2, seizures, benign neonatal, 2, BFNS2, convulsions, benign familial neonatal, 2

7 clinical trials for this condition and its sub-types.

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Broader categories

Disease (717) Epilepsy (447) Nervous system disorder (243) Hereditary disease (188) Brain disorder (131) Central nervous system disorder (115) Human disease (15) Hereditary neurological disease (6) Disease of genetic or genomic mechanism (2) Epilepsy syndrome (2)
Trials to join now! 4 Not yet finished but already full! 2 Completed 1
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  • Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test

    Diagnosis Completed

    This study is testing whether a computer tool called BioEP can detect signs of seizure susceptibility in standard EEG recordings from children with epilepsy. Researchers will analyze past EEGs from 530 children aged 2 to 18 who already have an epilepsy diagnosis. The goal is to s…

    Sponsor: Neuronostics Ltd • Aim: Diagnosis

    Last updated Aug 01, 2026 00:00 UTC

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