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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. Juvenile myoclonic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Juvenile_myoclonic_epilepsy

    Download as PDF; Printable version; ... is a form of hereditary, ... Approximately 15% of children with childhood absence epilepsy and juvenile absence epilepsy ...

  4. Absence seizure - Wikipedia

    en.wikipedia.org/wiki/Absence_seizure

    Juvenile Myoclonic Epilepsy (JME), also referred to as Janz Syndrome and Impulsive Petit Mal, is a form of epilepsy that is characterized by absence, Myoclonic, and Generalized Tonic-Clonic Seizures. This epilepsy variant is marked by its idiopathic and hereditary characteristics, as well as its generalization across seizures.

  5. 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.

  6. Idiopathic generalized epilepsy - Wikipedia

    en.wikipedia.org/.../Idiopathic_generalized_epilepsy

    Also known as Janz syndrome, juvenile myoclonic epilepsy (JME) is a common form of epilepsy, accounting for ~10% of all cases and ~25% of cases of idiopathic generalized epilepsies. Many children with CAE go on to develop JME. JME first presents between the ages of 12 and 18 with prominent myoclonic seizures.

  7. Epilepsy syndromes - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_syndromes

    Syndromes are characterized into 4 groups based on epilepsy type: [1] a. Generalized onset epilepsy syndromes. These epilepsy syndromes have only generalized-onset seizures and include both the idiopathic generalized epilepsies (specifically childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy and epilepsy with generalized tonic- clonic seizures alone), as well as ...

  8. Myoclonic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_epilepsy

    Myoclonic epilepsy refers to a family of epilepsies that present with myoclonus. When myoclonic jerks are occasionally associated with abnormal brain wave activity, it can be categorized as myoclonic seizure. If the abnormal brain wave activity is persistent and results from ongoing seizures, then a diagnosis of myoclonic epilepsy may be ...

  9. Juvenile absence epilepsy - Wikipedia

    en.wikipedia.org/?title=Juvenile_absence...

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