PhenomeGene — Human Disease Gene Website SeriesGRIN2A

Families

Two third of affected individuals known so far have developmental delay preceding intellectual disability of various degree, ranging from mild to severe.

Epilepsy is seen in nearly 90% of affected individuals with numerous possible semiologies. Additional features are speech disorders, muscular hypotonia, movement disorders, autism spectrum disorder and/or other behavior or psychiatric problems, including schizophrenia.