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  2. Juvenile myoclonic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Juvenile_myoclonic_epilepsy

    Absence seizures are believed to be least common, with an estimated prevalence between 10% and 40%. [13] [10] [14] Seizures associated with JME tend to take place 30 minutes to an hour after waking up in the morning. [10] Common triggers for JME seizures include lack of sleep, alcohol consumption, emotional stress, anxiety, and fatigue.

  3. 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 ...

  4. 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 ...

  5. 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]

  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. Benign infantile epilepsy - Wikipedia

    en.wikipedia.org/wiki/Benign_infantile_epilepsy

    Benign infantile epilepsy (BIE), also known as benign infantile seizures (BIS), is an epilepsy syndrome of which several forms have been described. The International League Against Epilepsy (ILAE) classify two main forms of the syndrome (familial and nonfamilial) [ 1 ] though several other forms have been described in the academic literature.

  8. Generalized epilepsy - Wikipedia

    en.wikipedia.org/wiki/Generalized_epilepsy

    Generalized epilepsy is a form of epilepsy characterised by generalised seizures with no apparent cause. [1] Generalized seizures, as opposed to focal seizures, are a type of seizure that impairs consciousness and distorts the electrical activity of the whole or a larger portion of the brain (which can be seen, for example, on electroencephalography, EEG).

  9. Myoclonic astatic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_astatic_epilepsy

    Myoclonic seizures: seizures with rapid, brief contractions of muscles. Atonic seizures: seizures with a sudden loss of muscle tone, often resulting in sudden collapse. These are also called drop seizures or astatic seizures. Absence seizures: a generalized seizure characterized by staring off and occasionally some orofacial automatisms.

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