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GRIN2A-related complex neurodevelopmental disorder

A group of neurological and neurodevelopmental disorders caused by variants in the GRIN2A gene, characterized by a broad spectrum of symptoms including developmental delay or intellectual disability, epilepsy, speech and language impairments, movement disorders, and neuropsychiatric features.

0 trials tagged with this condition →

GRIN2A-related developmental and/or epileptic encephalopathy with spike-wave activation in sleep 0 trials
GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome 0 trials
GRIN2A-related self-limited epilepsy with centrotemporal spikes 0 trials
Landau-Kleffner syndrome 0 trials
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation 0 trials