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  2. 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 ...

  3. 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]

  4. Seizure - Wikipedia

    en.wikipedia.org/wiki/Seizure

    A seizure is a period of symptoms due to abnormally excessive or synchronous neuronal activity in the brain. [6] Outward effects vary from uncontrolled shaking movements involving much of the body with loss of consciousness (tonic-clonic seizure), to shaking movements involving only part of the body with variable levels of consciousness (focal seizure), to a subtle momentary loss of awareness ...

  5. Epileptic spasms - Wikipedia

    en.wikipedia.org/wiki/Epileptic_spasms

    Epileptic spasms is an uncommon-to-rare epileptic disorder in infants, children and adults. One of the other names of the disorder, West syndrome, is in memory of the English physician, William James West (1793–1848), who first described it in an article published in The Lancet in 1841. [2]

  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. Photosensitive epilepsy - Wikipedia

    en.wikipedia.org/wiki/Photosensitive_epilepsy

    Photosensitive epilepsy (PSE) is a form of epilepsy in which seizures are triggered by visual stimuli that form patterns in time or space, such as flashing lights, bold, regular patterns, or regular moving patterns. PSE affects approximately one in 4,000 people (5% of those with epilepsy).

  9. Causes of seizures - Wikipedia

    en.wikipedia.org/wiki/Causes_of_seizures

    Generally, seizures are observed in patients who do not have epilepsy. [ 1 ] There are many causes of seizures. Organ failure, medication and medication withdrawal, cancer, imbalance of electrolytes, hypertensive encephalopathy, may be some of its potential causes. [ 2 ] The factors that lead to a seizure are often complex and it may not be ...

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