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Updated: May 7, 2026

Author Spotlight: Advancing Pediatric Epilepsy Surgery in Children Through Novel Biomarkers and Enhanced Localization
Published on: September 20, 2024
Two patients with a GRIN2A mutation and childhood-onset epilepsy
1Division of Pediatric Neurology, Nationwide Children's Hospital, and The Ohio State University College of Medicine, Columbus, Ohio.
Mutations in the glutamate receptor ionotropic N-methyl-D-aspartate 2A (GRIN2A) gene are linked to epilepsy. These genetic changes can cause a wide range of clinical symptoms in affected individuals.
Area of Science:
- Neuroscience
- Genetics
- Neurology
Background:
- N-methyl-D-aspartate (NMDA) is a crucial neurotransmitter in the central nervous system.
- NMDA receptor dysfunction is implicated in epilepsy pathogenesis.
- Mutations in the glutamate receptor ionotropic N-methyl-D-aspartate 2A (GRIN2A) gene are associated with neuropsychiatric disorders, including epilepsy.
Observation:
- Two patients with confirmed GRIN2A mutations presented with epilepsy.
- The clinical presentation of epilepsy in these patients was observed.
Findings:
- GRIN2A mutations are associated with epilepsy.
- Individuals with GRIN2A mutations display a diverse spectrum of clinical manifestations.
Implications:
- Understanding the role of GRIN2A in epilepsy can aid in diagnosis and treatment.
- Further research into GRIN2A mutations may reveal novel therapeutic targets for epilepsy.
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