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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. Focal seizure - Wikipedia

    en.wikipedia.org/wiki/Focal_seizure

    Focal seizures (also called partial seizures [1] and localized seizures) are seizures that affect initially only one hemisphere of the brain. [2] [3] The brain is divided into two hemispheres, each consisting of four lobes – the frontal, temporal, parietal and occipital lobes. A focal seizure is generated in and affects just one part of the ...

  4. Seizure types - Wikipedia

    en.wikipedia.org/wiki/Seizure_types

    A seizure is a paroxysmal episode of symptoms or altered behavior arising from abnormal excessive or synchronous brain neuronal activity. [5] A focal onset seizure arises from a biological neural network within one cerebral hemisphere, while a generalized onset seizure arises from within the cerebral hemispheres rapidly involving both hemispheres.

  5. Panayiotopoulos syndrome - Wikipedia

    en.wikipedia.org/wiki/Panayiotopoulos_syndrome

    Syncope-like epileptic seizures (ictal syncope) with the child becoming "completely unresponsive and flaccid like a rag doll" occur in one fifth of the seizures. [7] More-conventional seizure symptoms often appear after the onset of autonomic manifestations. The child, who was initially fully conscious, becomes confused and unresponsive.

  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. 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 ...

  8. Seizure - Wikipedia

    en.wikipedia.org/wiki/Seizure

    Seizure prediction is a special case of seizure detection in which the developed systems is able to issue a warning before the clinical onset of the epileptic seizure. [ 76 ] [ 78 ] Computational neuroscience has been able to bring a new point of view on the seizures by considering the dynamical aspects.

  9. Absence seizure - Wikipedia

    en.wikipedia.org/wiki/Absence_seizure

    Absence seizures affect between 0.7 and 4.6 per 100,000 in the general population and 6 to 8 per 100,000 in children younger than 15 years. Childhood absence seizures account for 10% to 17% of all absence seizures. Onset is between 4 and 10 years and peaks at 5 to 7 years. It is more common in girls than in boys. [1]

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