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  2. 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 ...

  3. Absence seizure - Wikipedia

    en.wikipedia.org/wiki/Absence_seizure

    Absence seizures are also known to occur to patients with porphyria and can be triggered by stress or other porphyrin-inducing factors. Childhood Absence Epilepsy. Childhood absence epilepsy (CAE) is a type of idiopathic epilepsy characterized by its non-convulsive, generalized nature and a genetic origin influenced by multiple factors [20]

  4. Epilepsy in children - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_in_children

    Generalized 3 Hz spike and wave discharges in a child with childhood absence epilepsy. Epilepsy is a neurological condition of recurrent episodes of unprovoked epileptic seizures. A seizure is an abnormal neuronal brain activity that can cause intellectual, emotional, and social consequences.

  5. Epilepsy syndromes - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_syndromes

    Childhood absence epilepsy (CAE) is a genetic generalized epilepsy that affects children between the ages of 4 and 12 years of age, although peak onset is around five to six years old. These patients have recurrent absence seizures , brief episodes of unresponsive staring, sometimes with minor motor features such as eye blinking or subtle chewing.

  6. Idiopathic generalized epilepsy - Wikipedia

    en.wikipedia.org/.../Idiopathic_generalized_epilepsy

    This rare epilepsy has a wide age range of presentation (from the first year of life through the early teens). This epilepsy is characterized by absence seizures concurrent with myoclonic jerks, typically occurring several times daily. The genetics of this disorder have not been delineated. Seizures from this disorder often cease within 5 years.

  7. Epilepsy - Wikipedia

    en.wikipedia.org/wiki/Epilepsy

    The ability to categorize a case of epilepsy into a specific syndrome occurs more often with children since the onset of seizures is commonly early. [69] Less serious examples are benign rolandic epilepsy (2.8 per 100,000), childhood absence epilepsy (0.8 per 100,000) and juvenile myoclonic epilepsy (0.7 per 100,000). [69]

  8. Causes of seizures - Wikipedia

    en.wikipedia.org/wiki/Causes_of_seizures

    In children between the ages of 6 months and 5 years, a fever of 38 °C (100.4 °F) or higher may lead to a febrile seizure. [25] About 2-5% of all children will experience such a seizure during their childhood. [26] In most cases, a febrile seizure will not indicate epilepsy. [26] Approximately 40% of children who experience a febrile seizure ...

  9. Jeavons syndrome - Wikipedia

    en.wikipedia.org/wiki/Jeavons_Syndrome

    Eyelid myoclonia with or without absences is a form of epileptic seizure manifesting with myoclonic jerks of the eyelids with or without a brief absence. These are mainly precipitated by closing of the eyes and lights. [1] [2] Eyelid myoclonia is the defining seizure type of Jeavons syndrome. [3]

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