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Febrile convulsions occur in at least 3% of children , between the age of 6 months and 5 years . The seizure is typically generalized and occurs in association with fevers. Intracranial infections such as meningitis must be excluded. The risk factors for development of epilepsy as a complication of febrile seizure include a positive family history of epilepsy, initial febrile convulsions before 9 mo of age, a prolonged or atypical febrile seizure , delayed developmental milestones, and abnormal neurologic findings. The incidence of epilepsy is 9% when several risk factors are present and 1% in children who have no risk factors .
Benign epilepsy with Rolandic foci: has an onset between 2 and 12 years, is maximal between 7 and 10, and stops by 13 years. The attacks are clonic , partially sensorimotor affecting the face,  bulbal muscles, hand, and arm, and they occur particularly on waking .
Benign occipital epilepsy: some children with typical partial seizures with visual phenomena, postictal headache, and migrainous characteristics have a benign prognosis, but others have a poorer cognitive and seizure outcome, and some have lesions .
Early myoclonic epilepsies:  separation of early myoclonic epilepsies into benign and malignant outcomes may not be possible early .
Absence seizures: range from a benign self - limiting condition to part of a malignant syndrome of multiple seizure types, particularly the Lennox - Gastaut syndrome. The rate of tonic-clonic seizures in adult life, can be predicted by the expected adverse factors: history of tonic-clonic seizures, IQ< 90, and a family history of seizures. Seizures continue in about 10% of cases with no adverse factors or only one and in 100% of cases with three adverse factors.