Progressive myoclonic epilepsy type 6

MONDO:0013526

Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the GOSR2 gene.

Also known as: EPM6, GOSR2 progressive myoclonic epilepsy, GOSR2-related progressive myoclonus ataxia, North Sea progressive myoclonus epilepsy, PME type 6, epilepsy, progressive myoclonic 6, epilepsy, progressive myoclonic, type 6, progressive myoclonic epilepsy caused by mutation in GOSR2

7 clinical trials for this condition and its sub-types, 0 tagged with Progressive myoclonic epilepsy type 6 itself.

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↑ Progressive myoclonus epilepsy (12)

Including sub-types (7) Tagged with Progressive myoclonic epilepsy type 6 (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

Progressive myoclonic epilepsy type 6

Where it sits in the disease tree

Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test