{"id":227,"date":"2017-07-01T20:15:15","date_gmt":"2017-07-01T20:15:15","guid":{"rendered":"https:\/\/docneuro.jz7sunfr-liquidwebsites.com\/absence-epilepsy\/"},"modified":"2020-01-20T20:44:59","modified_gmt":"2020-01-21T02:44:59","slug":"absence-epilepsy","status":"publish","type":"post","link":"https:\/\/docneuro.com\/absence-epilepsy\/","title":{"rendered":"Absence Epilepsy"},"content":{"rendered":"

Absence epilepsy is a type of primary generalized epilepsy in children, and usually presents as staring spells. <\/p>\n

Clinical Presentation of Absence Epilepsy<\/h3>\n

Childhood absence epilepsy develops in children, with a peak onset of 6 years old. Development of these seizures at an age of 10-12 is more consistent with the juvenile subtype or juvenile myoclonic epilepsy<\/a> rather than the typical childhood absence. Seizures have a sudden onset and abrupt termination of unresponsiveness. The seizures consist of staring spells, often associated with repetitive eyelid movements or oral automatisms. The events last for seconds at a time, typical around 10 seconds. The seizures can be triggered by hyperventilation, and in the pediatrician’s office seizures can provoked by having the child blow into a pinwheel or blow a tissue.<\/p>\n

3 Hz Spike and Wave Discharges on EEG<\/h3>\n
\"petit
3 Hz spike and wave EEG seen with absence epilepsy<\/figcaption><\/figure>\n

The classic EEG finding in absence seizures is an ictal pattern consisting of 3-Hz generalized spike-wave discharges. An example of this pattern is shown below.<\/p>\n

Pathology and Genetics of Absence Epilepsy<\/h3>\n

Multiple genetic mutations have been associated with this disorder, although not all genetic mutations have been identified. The best described mutations are in calcium channels, chloride channels, GABA-A receptors, and GABA-B receptors. The 3 Hz spike and wave discharges are thought to reflect a synchronized thalamocortical network. T-type calcium channels in the thalamus are thought to be an important component in the epileptic circuit.<\/p>\n

Treatment of Absence Seizures<\/h3>\n

The first-line therapy for absence seizures<\/a> is ethosuximide. If ineffective, valproic acid, lamotrigine and levetiracetam can be tried. Several anti-seizure medications are thought to worsen absence seizures, and should be avoided. These include carbamazepine, vigabatrin, tiagabine and phenytoin.<\/p>\n

Prognosis<\/h3>\n

The majority of children with absence epilepsy have spontaneous remission of the seizures by the early teenage years. However, the ~1\/3 of patients who do not enter remission typically progress to have Juvenile Myoclonic Epilepsy (JME).<\/p>\n

Petit mal seizures<\/h3>\n

The term “petit mal” is often used to describe staring seizures without convulsions, but this term is no longer considered an official descriptor of absence seizures.<\/p>\n\n\n

<\/p>\n","protected":false},"excerpt":{"rendered":"

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