Absence Seizures

Absence seizures are short seizures with behavioural arrest and generalised 3-Hertz spike-and-wave discharges on EEG. Absence seizures occur in multiple genetic generalized epilepsies, including Childhood Absence Epilepsy (CAE), juvenile absence epilepsy (JAE), and Juvenile Myoclonic Epilepsy (JME).

Pathophysiology

Fig. 1: Thalamocortical circuitry involved in the pathogenesis of absence seizures. Thalamic relay (TR) neurons exhibit spike-wave discharges that result from activation of T-type Ca++ channels, followed by hyperpolarization mediated by GABA released from thalamic reticular (NRT) neurons.

Hence T-type calcium channel suppressors like ethosuximide and valproate are used for treating absence seizures. GABA-A agonists like benzodiazepines that preferentially activate thalamic nucleus reticularis neurons can also decrease absence seizures. However Vigabatrin, which increases GABA-B activity will increase absence seizures. Other medications which can worsen absence seizures are sodium channel blockers like Carbamazepine, phenytoin and gabapentin.


1. a Onat FY, van Luijtelaar G, Nehlig A, Snead OC3. The involvement of limbic structures in typical and atypical absence epilepsy. Epilepsy Res. 2013 Feb;103(2-3):111-23. doi: 10.1016/j.eplepsyres.2012.08.008. Epub 2012 Sep 16.
[PMID: 22989853] [DOI: 10.1016/j.eplepsyres.2012.08.008]