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  2. Epilepsy - Wikipedia

    en.wikipedia.org/wiki/Epilepsy

    Diagnosis of epilepsy can be difficult. A number of other conditions may present very similar signs and symptoms to seizures, including syncope, hyperventilation, migraines, narcolepsy, panic attacks and psychogenic non-epileptic seizures (PNES). [133] [134] In particular, syncope can be accompanied by a short episode of convulsions. [135]

  3. Seizure - Wikipedia

    en.wikipedia.org/wiki/Seizure

    Focal seizures affect a specific area of the brain, not both sides. [13] It may turn into a generalized seizure if the seizure spreads through the brain. [3] [13] [8] Consciousness may or may not be impaired. [3] [5] The signs and symptoms of these seizures depends on the location of the brain that is affected. Focal seizures usually consist of ...

  4. Temporal lobe epilepsy - Wikipedia

    en.wikipedia.org/wiki/Temporal_lobe_epilepsy

    Temporal lobe epilepsy is the most common type of focal onset epilepsy among adults. [1] Seizure symptoms and behavior distinguish seizures arising from the mesial temporal lobe from seizures arising from the lateral (neocortical) temporal lobe. [2] Memory and psychiatric comorbidities may occur.

  5. Occipital epilepsy - Wikipedia

    en.wikipedia.org/wiki/Occipital_epilepsy

    Seizures originate in the occipital lobe and account for 5 to 10 percent of all epileptic seizure types. Generally, this type of epilepsy can have an onset anywhere from 1–17 years old in children, but the patient prognosis is good. Since the event is located in the occipital lobe, symptoms may occur spontaneously and include visual stimuli.

  6. Frontal lobe epilepsy - Wikipedia

    en.wikipedia.org/wiki/Frontal_lobe_epilepsy

    The most common subdivision of epilepsy is symptomatic partial epilepsy, which causes simple partial seizures, and can be further divided into temporal and frontal lobe epilepsy. Although the exact number of cases of frontal lobe epilepsy is not currently known, it is known that FLE is the less common type of partial epilepsy, accounting for 20 ...

  7. Dravet syndrome - Wikipedia

    en.wikipedia.org/wiki/Dravet_syndrome

    Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic form of epilepsy, with prolonged seizures that are often triggered by hot temperatures or fever. [1]

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