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A seizure is a set of clinical symptoms due to abnormal electrical activity of the brain. Epilepsy is a syndrome where there have been recurrent unprovoked seizures or a single unprovoked seizure with findings to indicate that there is a comparable risk of subsequent seizure as would be seen in a patient with two unprovoked seizures. Therefore, all patients with epilepsy have seizures, whereas not all patients with seizures have epilepsy.
Seizures come in a variety of types with different clinical features. The classification scheme has evolved, and some authors and practitioners adhere to now-obsolete schemes. Because of this, neurologists need to be aware of the new accepted schemes and the parallels in prior terminology.
Seizures are first classified into generalized or focal onset. Generalized seizures are those that have a generalized onset, that is, the seizures did not start in a specific focus and then spread. These are subdivided into motor onset and nonmotor onset. Motor onset seizures would include the generalized tonic-clonic (GTC) seizures. Nonmotor onset seizures would include absence seizures.
Classification of epilepsies is complex, but for the purposes of localization and diagnosis it is appropriate to introduce it here. The seizure classification is first and most important.
Epilepsies are classified as focal, generalized, combination of focal and generalized, and unknown. This classification is based on the origin of the discharges that comprise the seizures. There are also classification strata based on whether the seizures are structural, genetic, metabolic, infectious, immune, or unknown, which are not pivotal for localization.
Classification of seizures is as follows:
Focal onset
Awareness
Aware
Impaired awareness
Onset
Motor onset
Nonmotor onset
Focal to bilateral tonic-clonic seizures
Generalized
Motor onset
Nonmotor onset (absence)
Unknown onset
Motor onset
Tonic-clonic
Epileptic spasms
Nonmotor onset
Unclassified
Classification of epilepsies is as follows:
Epilepsy types
Focal
Generalized
Combination of focal and generalized
Unknown
Etiologies
Structural
Genetic
Infectious
Metabolic
Immune
Unknown
Epilepsy syndromes
Idiopathic generalized epilepsies
Childhood absence
Juvenile absence
Juvenile myoclonic
Generalized tonic-clonic
Self-limited focal epilepsies
With centrotemporal spikes
Self-limited occipital epilepsies
Other self-limited frontal, temporal, or parietal epilepsies
GTC seizures usually begin abruptly with loss of consciousness that is followed by generalized tonic and then clonic activity. If the GTC arises in a patient with juvenile myoclonic epilepsy (JME), myoclonic jerks may precede the GTC phase. The patient’s eyes are usually partly open, and their mouth is often open. Their head may turn to either side, without the seizure being considered a focal onset type. Postictal sleepiness and confusion are expected.
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