enow.com Web Search

  1. Ads

    related to: intractable epilepsy life expectancy
    • Epilepsy Care

      Options for Epilepsy Management.

      Access a Free Treatment Guide.

    • Epilepsy Diagnosis

      Neurological Diagnoses & Care.

      Get the Free Epilepsy Guide.

Search results

  1. Results from the WOW.Com Content Network
  2. Pachygyria - Wikipedia

    en.wikipedia.org/wiki/Pachygyria

    Lissencephaly is present in 1 of 85,470 births and the life span of those affected is short as only a few survive past the age of 20. [1] ... intractable epilepsy;

  3. 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] It is very difficult to treat with anticonvulsant medications.

  4. Management of drug-resistant epilepsy - Wikipedia

    en.wikipedia.org/wiki/Management_of_drug...

    Drug-resistant epilepsy (DRE), also known as refractory epilepsy, intractable epilepsy, or pharmacoresistant epilepsy refers to a state in which an individual with a diagnosis of epilepsy is unresponsive to multiple first line therapies.

  5. Progressive myoclonus epilepsy - Wikipedia

    en.wikipedia.org/wiki/Progressive_myoclonus_epilepsy

    MEAK is a form of progressive myoclonus epilepsy that typically begins between the ages of 3 and 15 years (the average of onset is 10 years). The first symptoms may include ataxia and myoclonus (unsteadiness and difficulty coordinating movements), along with generalized tonic-clonic ("grand mal") seizures.

  6. Lennox–Gastaut syndrome - Wikipedia

    en.wikipedia.org/wiki/Lennox–Gastaut_syndrome

    LGS is seen in approximately 4% of children with epilepsy, and is more common in males than in females. [13] Usual onset is between the ages of three and five. [7] Children can have no neurological problems prior diagnosis, or have other forms of epilepsy. West syndrome is diagnosed in 20% of patients before it evolves into LGS at about 2 years ...

  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).

  8. Corpus callosotomy - Wikipedia

    en.wikipedia.org/wiki/Corpus_callosotomy

    The diminished life expectancy associated with epilepsy has been documented by population-based studies in Europe. In the UK and Sweden, the relative mortality rate of epileptic patients (patients whose epilepsy was not under control from medical or other surgical therapies and who continued to have the disease) increased two- and threefold ...

  9. Focal cortical dysplasia - Wikipedia

    en.wikipedia.org/wiki/Focal_cortical_dysplasia

    Focal cortical dysplasia is a common cause of intractable epilepsy in children and is a frequent cause of epilepsy in adults. There are three types of FCD with subtypes, including type 1a, 1b, 1c, 2a, 2b, 3a, 3b, 3c, and 3d, each with distinct histopathological features.

  1. Ads

    related to: intractable epilepsy life expectancy