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Mowat-Wilson syndrome due to a ZEB2 point mutation

MONDO:0016856

Also known as: Hirschsprung disease and intellectual disability due to a ZEB2 point mutation

7 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) Neurodevelopmental disorder (147) Intellectual disability (133) Brain disorder (125) Central nervous system disorder (107) Syndromic disease (25) Human disease (14)

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