GRIN2A-related complex neurodevelopmental disorder
MONDO:1060139A 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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Browse by category →Sub-types of GRIN2A-related complex neurodevelopmental disorder
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Landau-Kleffner syndrome 0 trials