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• W2997551504 abstract "Epileptic spasm (ES) is one of the seizure types which is difficult to treat. Next-generation sequencing has facilitated rapid gene discovery that is linked to ES and GRIN2A being one of them. Genotype-driven precision medicine is on the horizon and is a targeted treatment approach toward the precise molecular cause of the disease. GRIN2A gene encodes for a subunit of N-methyl-D-aspartate (NMDA) receptor and it has been suggested from in vitro studies and few case reports that memantine, a NMDA receptor antagonist, was shown to reduce seizures in patients with GRIN2A mutations. Here, we describe a patient with a novel GRIN2A mutation and severe drug-resistant ES who became seizure free with memantine." @default.
• W2997551504 created "2020-01-10" @default.
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• W2997551504 date "2019-12-24" @default.
• W2997551504 modified "2023-09-26" @default.
• W2997551504 title "GRIN2A-Related Severe Epileptic Encephalopathy Treated with Memantine: An Example of Precision Medicine" @default.
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• W2997551504 doi "https://doi.org/10.1055/s-0039-3401028" @default.
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