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Neonatal/infantile-onset self-limited epilepsy syndrome

MONDO:0800488

An epilepsy syndrome characterized by the onset of seizures in neonates/infants where there is a high likelihood of spontaneously remitting at a predictable age.

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

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Sub-types

Genetic epilepsy with febrile seizures plus spectrum (0) Myoclonic epilepsy in infancy (0) Self-limited familial infantile epilepsy (0) Self-limited familial neonatal-infantile epilepsy (0) Self-limited neonatal seizures (0)

Broader categories

Disease (680) Epilepsy (438) Nervous system disorder (231) Brain disorder (125) Central nervous system disorder (107) Human disease (14) Epilepsy syndrome (2) Neonatal/infantile epilepsy syndrome (1) Disease by body system or component (0)

Trials to join now! 4 Not yet finished but already full! 2 Completed 1

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