GRIN2A-related complex neurodevelopmental disorder

MONDO:1060139

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.

1 clinical trial for this condition and its sub-types, 0 tagged with GRIN2A-related complex neurodevelopmental disorder itself.

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Sub-types of GRIN2A-related complex neurodevelopmental disorder

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

Including sub-types (1) Tagged with GRIN2A-related complex neurodevelopmental disorder (0)

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