{"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
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 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 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>\n3 Hz Spike and Wave Discharges on EEG<\/h3>\n
Pathology and Genetics of Absence Epilepsy<\/h3>\n
Treatment of Absence Seizures<\/h3>\n