Pathogenic variants (“mutations”) in the GRIN2A gene cause a spectrum of neurodevelopmental disorders that can include childhood-onset epilepsy, developmental delays, and speech and language disorders.

2016年9月29日 · GRIN2A-related disorders encompass a broad phenotypic spectrum that includes developmental delay evolving to intellectual disability (DD/ID), epilepsy, speech and language disorders, movement disorders, and neuropsychiatric disorders. Intellect ranges from normal to profoundly impaired.

2025年3月30日 · GRIN2A (Glutamate Ionotropic Receptor NMDA Type Subunit 2A) is a Protein Coding gene. Diseases associated with GRIN2A include Epilepsy, Focal, With Speech Disorder And With Or Without Impaired Intellectual Development and Landau-Kleffner Syndrome.

GRIN2A variants are associated with epileptic encephalopathies such as Landau-Kleffner Syndrome (LKS) and Continuous Spike and Wave During Sleep (CSWS). They are also associated with other encephalopathic phenotypes. GRIN2A variants have also been identified in people with focal epilepsies.

2019年1月1日 · Alterations of the N-methyl-d-aspartate receptor (NMDAR) subunit GluN2A, encoded by GRIN2A, have been associated with a spectrum of neurodevelopmental disorders with prominent speech-related features, and epilepsy.

The GRIN2A gene provides instructions for making a protein called GluN2A (formerly known as NR2A). This protein is found in nerve cells (neurons) in the brain and spinal cord, including regions of the brain involved in speech and language.

This review compares and contrasts the available information describing the clinical and functional consequences of genetic variations in GRIN2A and GRIN2B.

2024年2月14日 · GRIN2A-related disorder is characterized by either mild-to-profound developmental delay / intellectual disability in two thirds of affected individuals. Other common manifestations are speech disorders, epilepsy, muscular hypotonia, movement disorders, spasticity, feeding difficulties, and behavior problems.

2023年9月19日 · Sequencing data shows that 43% (297/679) of all currently known NMDAR disease-associated genetic variants are within the GRIN2A gene, which encodes the GluN2A subunit.

GRIN2A mutation is associated with epilepsy-aphasia spectrum disorders but with a relatively low rate. Lifetime mood disorder emerged as a more significant factor for suicidal ideation in systemic lupus erythematosus compared with NR2A gene polymorphism main and interaction effects.