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  2. Epilepsy in children - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_in_children

    The epileptic seizure in the vast majority of pediatric epilepsy patients is ephemeral, and symptoms typically subside on their own after the seizure comes to an end, but some children experience what is known as a “seizure cluster," in which the first seizure is followed by a second episode approximately six hours later.

  3. Idiopathic childhood occipital epilepsy of Gastaut - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_childhood...

    Thus, some children may have numerous diurnal visual seizures and only a few seizures that are exclusively nocturnal or occur on awakening. [citation needed] Frequency of seizures: If untreated, patients experience frequent and brief visual seizures (often several every day or weekly). However, propagation to other seizure manifestations, such ...

  4. Febrile seizure - Wikipedia

    en.wikipedia.org/wiki/Febrile_seizure

    Simple febrile seizures involve an otherwise healthy child who has at most one tonic-clonic seizure lasting less than 15 minutes in a 24-hour period. [1] Complex febrile seizures have focal symptoms, last longer than 15 minutes, or occur more than once within 24 hours. [5] About 80% are classified as simple febrile seizures. [6]

  5. Childhood absence epilepsy - Wikipedia

    en.wikipedia.org/wiki/Childhood_absence_epilepsy

    Childhood absence epilepsy (CAE), formerly known as pyknolepsy, is an idiopathic generalized epilepsy which occurs in otherwise normal children. The age of onset is between 4–10 years with peak age between 5–7 years. Children have absence seizures which although brief (~4–20 seconds), they occur frequently, sometimes in the hundreds per ...

  6. Rolandic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Rolandic_epilepsy

    Benign Rolandic epilepsy or self-limited epilepsy with centrotemporal spikes (formerly benign childhood epilepsy with centrotemporal spikes (BECTS)) is the most common epilepsy syndrome in childhood. [ 1 ] [ 2 ] Most children will outgrow the syndrome (it starts around the age of 3–13 with a peak around 8–9 years and stops around age 14 ...

  7. Occipital epilepsy - Wikipedia

    en.wikipedia.org/wiki/Occipital_epilepsy

    Seizures originate in the occipital lobe and account for 5 to 10 percent of all epileptic seizure types. Generally, this type of epilepsy can have an onset anywhere from 1–17 years old in children, but the patient prognosis is good. Since the event is located in the occipital lobe, symptoms may occur spontaneously and include visual stimuli.

  8. Seizure - Wikipedia

    en.wikipedia.org/wiki/Seizure

    Systemic infection with high fever is a common cause of seizures, especially in children. [3] [25] These are called febrile seizures and occur in 2–5% of children between the ages of six months and five years. [26] [25] Acute infection of the brain, such as encephalitis or meningitis are also causes of seizures. [3]

  9. Panayiotopoulos syndrome - Wikipedia

    en.wikipedia.org/wiki/Panayiotopoulos_syndrome

    Panayiotopoulos syndrome (named after C. P. Panayiotopoulos) is a common idiopathic childhood-related seizure disorder that occurs exclusively in otherwise normal children (idiopathic epilepsy) and manifests mainly with autonomic epileptic seizures and autonomic status epilepticus. [1]

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