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Up to: Childhood absence epilepsy · Febrile seizures, familial · Generalized epilepsy with febrile seizures plus
Febrile seizures, familial, 8
A childhood absence epilepsy that is characterized by mutations in the GABRG2 gene, which cause a spectrum of seizure disorders, ranging from early-onset isolated febrile seizures (FS) to childhood absence epilepsy (CAE) to generalized epilepsy with febrile seizures plus, type 3 (GEFS+3), which tends to represent a more severe phenotype.
This condition has no sub-types.