enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Myoclonic astatic epilepsy - Wikipedia

    en.wikipedia.org/wiki/Myoclonic_astatic_epilepsy

    Myoclonic seizures: seizures with rapid, brief contractions of muscles. Atonic seizures: seizures with a sudden loss of muscle tone, often resulting in sudden collapse. These are also called drop seizures or astatic seizures. Absence seizures: a generalized seizure characterized by staring off and occasionally some orofacial automatisms.

  3. 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]

  4. Hemimegalencephaly - Wikipedia

    en.wikipedia.org/wiki/Hemimegalencephaly

    Left-sided hemimegalencephaly in a person with neurofibromatosis [1] Specialty: Neurology, rheumatology Symptoms: Frequent seizures often resistant to medicine: Usual onset: Congenital: Duration: Long term: Treatment: Hemispherectomy: Medication: Anti-epileptic drugs

  5. Status epilepticus - Wikipedia

    en.wikipedia.org/wiki/Status_epilepticus

    The seizures can be of the tonic–clonic type, with a regular pattern of contraction and extension of the arms and legs, or of types that do not involve contractions, such as absence seizures or complex partial seizures. [1] Status epilepticus is a life-threatening medical emergency, particularly if treatment is delayed. [1]

  6. Idiopathic generalized epilepsy - Wikipedia

    en.wikipedia.org/.../Idiopathic_generalized_epilepsy

    Juvenile absence epilepsy is similar to CAE but has an onset between ages 9 and 13. Other differences are that patients with this disorder have less frequent but longer absence seizures than those with CAE. There are a number of possible genetic loci for this disorder, though no causative genes have been demonstrated.

  7. SYNGAP1-related intellectual disability - Wikipedia

    en.wikipedia.org/wiki/SYNGAP1-related...

    The 2023 edition of ICD-10-CM F78.A1 became effective on October 1, 2022. This is the American ICD-10-CM version of F78.A1 - other international versions of ICD-10 F78.A1 may differ. On August 11, 2021, SYNGAP1 -related Disorders was included in the Social Security Administration list of diseases for Compassionate Use .

  8. Generalized epilepsy - Wikipedia

    en.wikipedia.org/wiki/Generalized_epilepsy

    Generalized epilepsy is a form of epilepsy characterised by generalised seizures with no apparent cause. [1] Generalized seizures, as opposed to focal seizures, are a type of seizure that impairs consciousness and distorts the electrical activity of the whole or a larger portion of the brain (which can be seen, for example, on electroencephalography, EEG).

  9. 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 ...