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  2. Idiopathic generalized epilepsy - Wikipedia

    en.wikipedia.org/.../Idiopathic_generalized_epilepsy

    Idiopathic generalized epilepsy (IGE) is a group of epileptic disorders that are believed to have a strong underlying genetic basis. IGE is considered a subgroup of Genetic Generalized Epilepsy (GGE). [1] Patients with an IGE subtype are typically otherwise normal and have no structural brain abnormalities.

  3. Epilepsy - Wikipedia

    en.wikipedia.org/wiki/Epilepsy

    Juvenile idiopathic epilepsy (JIE) in foals is a condition with varying outcomes, depending on the severity and management of the condition. Some foals eventually outgrow the condition without significant long-term effects, while others may face severe consequences, including death or lifelong complications, if left untreated.

  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. Seizure - Wikipedia

    en.wikipedia.org/wiki/Seizure

    A seizure is a sudden change in behavior, movement or consciousness due to abnormal electrical activity in the brain. [3] [6] Seizures can look different in different people.. It can be uncontrolled shaking of the whole body (tonic-clonic seizures) or a person spacing out for a few seconds (absence seizure

  6. Idiopathic childhood occipital epilepsy of Gastaut - Wikipedia

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

    Idiopathic childhood occipital epilepsy of Gastaut (ICOE-G) is a pure but rare form of idiopathic occipital epilepsy that affects otherwise normal children and adolescents. [1] It is classified amongst benign idiopathic childhood focal epilepsies such as rolandic epilepsy and Panayiotopoulos syndrome .

  7. Myoclonic astatic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_astatic_epilepsy

    Myoclonic astatic epilepsy (MAE), also known as myoclonic atonic epilepsy or Doose syndrome, and renamed "Epilepsy with myoclonic-atonic seizures" in the ILAE 2017 classification, is a generalized idiopathic epilepsy. It is characterized by the development of myoclonic seizures and/or myoclonic astatic seizures. Some of the common monogenic ...

  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 epilepsy - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_epilepsy

    Seizures usually begin around puberty and usually have a genetic basis. [4] Seizures can be stimulus-selective, with flashing lights being one of the most common triggers. [4] Juvenile myoclonic epilepsy (JME) is a prevalent and typical form of idiopathic generalized epilepsy (IGE) syndrome.

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