Table 3.

Selected Genes of Interest in the Differential Diagnosis of GRIA2-Related Neurodevelopmental Disorder

GeneDisorderMOI
FOXG1 Rett syndrome, congenital variant (See FOXG1 Syndrome.)AD
GRIA1 GRIA1-NDD (OMIM 619931, 619927)AD
AR
GRIA3 GRIA3-NDD (OMIM 300699)XL
GRIA4 GRIA4-NDD (OMIM 617864)AD
GRIN1 GRIN1-NDD AD
AR
GRIN2A GRIN2A-NDD (See GRIN2A-Related Speech Disorders and Epilepsy.)AD
MECP2 MECP2 disorders XL

AD = autosomal dominant; AR = autosomal recessive; MOI = mode of inheritance; NDD = neurodevelopmental disorder; XL = X-linked

From: GRIA2-Related Neurodevelopmental Disorder

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