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Up to: Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy

Febrile infection-related epilepsy syndrome

A rare, potentially fatal, epileptic encephalopathy characterized by explosive-onset of recurrent multifocal and bilateral tonic-clonic seizures following an unspecific febrile illness. The syndrome develops without a clear acute structural, toxic or metabolic cause, in a patient without previous epilepsy. FIRES is a subgroup of new-onset refractory status epilepticus (NORSE), and requires a preceding febrile infection as a mandatory feature.

1 trial tagged with this condition →

This condition has no sub-types.