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  2. Epilepsy in children - Wikipedia

    en.wikipedia.org/wiki/Epilepsy_in_children

    The epileptic seizure in the vast majority of pediatric epilepsy patients is ephemeral, and symptoms typically subside on their own after the seizure comes to an end, but some children experience what is known as a “seizure cluster," in which the first seizure is followed by a second episode approximately six hours later.

  3. Neonatal seizure - Wikipedia

    en.wikipedia.org/wiki/Neonatal_seizure

    According to the International League against Epilepsy (ILAE), seizures are defined as excessive or synchronous neuronal activity in the brain that is manifested as signs or symptoms. As per the classification system by the American Clinical Neurophysiology Society, seizures can be classified into electroclinical (clinical signs of a seizure ...

  4. Lennox–Gastaut syndrome - Wikipedia

    en.wikipedia.org/wiki/Lennox–Gastaut_syndrome

    The diagnosis of LGS should be suspected in children less than 8 years old with seizures of multiple types that cannot be treated with anti-seizure medications. Because of high risk of irreversible brain damage in early stages of syndrome (particularly in infants and young children), early diagnosis is essential.

  5. Focal seizure - Wikipedia

    en.wikipedia.org/wiki/Focal_seizure

    A simple partial seizure may go unnoticed by others or shrugged off by the patient as merely a "funny turn." Focal aware seizures usually start suddenly and are very brief, typically lasting 60 to 120 seconds. [10] [failed verification] Some common symptoms of a simple partial seizure are: [7] [failed verification] preserved consciousness

  6. Malignant migrating partial seizures in infancy - Wikipedia

    en.wikipedia.org/wiki/Malignant_migrating...

    Malignant migrating partial seizures of infancy (MMPSI) is a rare epileptic syndrome that onsets before 6 months of age, commonly in the first few weeks of life. [3] Once seizures start, the site of seizure activity repeatedly migrates from one area of the brain to another, with few periods of remission in between.

  7. Ohtahara syndrome - Wikipedia

    en.wikipedia.org/wiki/Ohtahara_syndrome

    Ohtahara syndrome (OS), also known as Early Infantile Developmental & Epileptic Encephalopathy (EIDEE) [2] is a progressive epileptic encephalopathy.The syndrome is outwardly characterized by tonic spasms and partial seizures within the first few months of life, [3] and receives its more elaborate name from the pattern of burst activity on an electroencephalogram (EEG).

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