GABRG2 Variants Associated with Febrile Seizures.
Ciria C HernandezYanwen ShenNingning HuWangzhen ShenVinodh NarayananKeri RamseyWen HeLiping ZouRobert L MacdonaldPublished in: Biomolecules (2023)
Febrile seizures (FS) are the most common form of epilepsy in children between six months and five years of age. FS is a self-limited type of fever-related seizure. However, complicated prolonged FS can lead to complex partial epilepsy. We found that among the GABA A receptor subunit ( GABR ) genes, most variants associated with FS are harbored in the γ2 subunit ( GABRG2 ). Here, we characterized the effects of eight variants in the GABA A receptor γ2 subunit on receptor biogenesis and channel function. Two-thirds of the GABRG2 variants followed the expected autosomal dominant inheritance in FS and occurred as missense and nonsense variants. The remaining one-third appeared as de novo in the affected probands and occurred only as missense variants. The loss of GABA A receptor function and dominant negative effect on GABA A receptor biogenesis likely caused the FS phenotype. In general, variants in the GABRG2 result in a broad spectrum of phenotypic severity, ranging from asymptomatic, FS, genetic epilepsy with febrile seizures plus (GEFS+), and Dravet syndrome individuals. The data presented here support the link between FS, epilepsy, and GABRG2 variants, shedding light on the relationship between the variant topological occurrence and disease severity.