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Familial temporal lobe epilepsy 5

MONDO:0013741

A temporal lobe epilepsy that has material basis in heterozygous mutation in the CPA6 gene on chromosome 8q13.

Also known as: ETL5, epilepsy, familial temporal lobe, type 5, familial temporal lobe epilepsy type 5, epilepsy, familial temporal lobe, 5

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

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Broader categories

Disease (680) Epilepsy (438) Nervous system disorder (231) Hereditary disease (176) Brain disorder (125) Central nervous system disorder (107) Focal epilepsy (99) Temporal lobe epilepsy (30) Childhood-onset epilepsy syndrome (18) Human disease (14)

Trials to join now! 7 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