Please sign in to follow a disease.

Developmental and epileptic encephalopathy 94

MONDO:0014150

An idiopathic generalized epilepsy characterized by onset of multiple seizure types in the first few years of life and associated with poor prognosis. Affected individuals have cognitive regression and intellectual disability.

Also known as: DEE94, EEOC, childhood onset epileptic encephalopathy, developmental and epileptic encephalopathy 94, CHCHD10-related disorders, CHD2 myoclonic encephalopathy, childhood-onset epileptic encephalopathy, epileptic encephalopathy, childhood-onset

19 clinical trials for this condition and its sub-types, 1 tagged with Developmental and epileptic encephalopathy 94 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Lennox-Gastaut syndrome (27)

Including sub-types (19) Tagged with Developmental and epileptic encephalopathy 94 (1)

Not yet finished but already full! 1

Can mapping a rare Gene's effects pave the way to targeted epilepsy therapies?

Knowledge-focused Ongoing

This study follows children aged 6 to 21 who have a CNKSR2 gene mutation, which can cause epilepsy, language difficulties, and intellectual disability. Researchers will use brain scans, EEGs, and developmental tests to track how the condition changes over time. The goal is to cre…

Sponsor: University of California, San Francisco • Aim: Knowledge-focused

Last updated Jul 25, 2026 00:00 UTC

Developmental and epileptic encephalopathy 94

Where it sits in the disease tree

Can mapping a rare Gene's effects pave the way to targeted epilepsy therapies?