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  2. Generalized tonic–clonic seizure - Wikipedia

    en.wikipedia.org/wiki/Generalized_tonic–clonic...

    A generalized tonic–clonic seizure, commonly known as a grand mal seizure or GTCS, [1] is a type of generalized seizure that produces bilateral, convulsive tonic and clonic muscle contractions. Tonic–clonic seizures are the seizure type most commonly associated with epilepsy and seizures in general and the most common seizure associated ...

  3. 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 ...

  4. Status epilepticus - Wikipedia

    en.wikipedia.org/wiki/Status_epilepticus

    40 per 100,000 people per year [2] Status epilepticus (SE), or status seizure, is a medical condition consisting of a single seizure lasting more than 5 minutes, or 2 or more seizures within a 5-minute period without the person returning to normal between them. [3][1] Previous definitions used a 30-minute time limit. [2]

  5. Anticonvulsant - Wikipedia

    en.wikipedia.org/wiki/Anticonvulsant

    Anticonvulsant. Anticonvulsants (also known as antiepileptic drugs, antiseizure drugs, or anti-seizure medications (ASM)) are a diverse group of pharmacological agents used in the treatment of epileptic seizures. [ 1 ] Anticonvulsants are also increasingly being used in the treatment of bipolar disorder [ 2 ][ 3 ] and borderline personality ...

  6. 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. [7]

  7. Juvenile myoclonic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Juvenile_myoclonic_epilepsy

    Juvenile myoclonic epilepsy (JME), also known as Janz syndrome or impulsive petit mal, is a form of hereditary, idiopathic generalized epilepsy, [ 1 ] representing 5–10% of all epilepsy cases. [ 2 ][ 3 ][ 4 ] Typically it first presents between the ages of 12 and 18 with myoclonic seizures (brief, involuntary, single or multiple episodes of ...

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