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  2. Seizure - Wikipedia

    en.wikipedia.org/wiki/Seizure

    Strokes, brain bleeds, and traumatic brain injury can all also lead to epilepsy if seizures re-occur. If the first seizure occurs more than 7 days following a stroke, there is a higher chance of the person developing epilepsy. [28] Post-stroke epilepsy accounts for 30%-50% of new epilepsy cases. [28]

  3. 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 ...

  4. Epilepsy in children - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_in_children

    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. Epilepsy affects children and adults of all ages and races, and is one of the most common neurological disorders of the nervous system. [1]

  5. Epilepsy - Wikipedia

    en.wikipedia.org/wiki/Epilepsy

    Epilepsy is a group of non-communicable neurological disorders characterized by recurrent epileptic seizures. [10] An epileptic seizure is the clinical manifestation of an abnormal, excessive, and synchronized electrical discharge in the neurons. [1] The occurrence of two or more unprovoked seizures defines epilepsy. [11]

  6. Rolandic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Rolandic_epilepsy

    Neurology. 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 ...

  7. Lennox–Gastaut syndrome - Wikipedia

    en.wikipedia.org/wiki/Lennox–Gastaut_syndrome

    Lennox–Gastaut syndrome (LGS) is a complex, rare, and severe childhood-onset epilepsy syndrome. It is characterized by multiple and concurrent seizure types including tonic seizure, cognitive dysfunction, and slow spike waves on electroencephalogram (EEG), which are very abnormal. [1] Typically, it presents in children aged 3–5 years and ...

  8. Generalized tonic–clonic seizure - Wikipedia

    en.wikipedia.org/wiki/Generalized_tonic–clonic...

    A generalized tonic–clonic seizure, commonly known as a grand mal seizure or GTCS, [1] is a type of generalized seizure that produces bilateral, convulsive tonic and clonic muscle contractions. Tonic–clonic seizures are the seizure type most commonly associated with epilepsy and seizures in general and the most common seizure associated ...

  9. 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).