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Idiopathic generalized epilepsy

Current Treatment Options in Neurology, 2004
Successful treatment of idiopathic generalized epilepsy begins with accurate seizure classification. Seizure types, such as absence, myoclonic, and primary generalized tonic-clonic seizures (PGTCS), often can be classified based on a detailed history and inter-ictal electroencephalogram (EEG).
Joseph E., Sullivan, Dennis J., Dlugos
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Primary generalized epilepsies

Current Treatment Options in Neurology, 2000
For pure childhood absence epilepsy (CAE), ethosuximide (ESM) remains the drug of first choice. Although valproic acid (VPA) is of equal efficacy, it is more toxic, and is reserved for those patients with accompanying convulsions. Lamotrigine (LTG) is effective as both add-on and monotherapy for CAE.
, Murphy, , Delanty
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Genetic Generalized Epilepsies

Journal of Clinical Neurophysiology, 2012
In the International League Against Epilepsy's most recent revision of classification and terminology, the term idiopathic epilepsy, previously used to describe those epilepsies whose cause was unknown, but presumed genetic, has been removed. It has been replaced by the term genetic epilepsy, only to be used to describe epilepsy in which the etiology ...
William B, Gallentine, Mohamad A, Mikati
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Cenobamate in Generalized Epilepsy and Combined Generalized and Focal Epilepsy

Neurology Clinical Practice, 2023
Cenobamate (CNB) is a United States Food and Drug Administration-approved antiseizure medication (ASM) for focal-onset seizures; however, its potential clinical effectiveness as a broad-spectrum ASM is not established. CNB has a proposed dual mechanism of action with preferential blockade of persistent sodium currents and positive allosteric modulation
Shruti Agashe   +8 more
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Generalized epilepsies

2019
Idiopathic generalized epilepsies (IGE) are characterized by normal background EEG activity and generalized interictal spike-and-wave discharges in the absence of any evidence of brain lesion. Absence epilepsies are the prototypes of IGEs. In childhood and juvenile absence epilepsies, by definition, all patients manifest absence seizures associated ...
Guerrini R., Marini C., Barba C.
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Idiopathic generalized epilepsies

2012
Abstract The idiopathic generalized epilepsies (IGEs) are a spectrum of epilepsy syndromes that are characterized by seizures of generalized onset, and by known or presumed genetic etiology. These syndromes occur frequently in adults and children aged above 2 years.
Amy, Kao, Pooja M, Rao
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Idiopathic generalized epilepsies

2013
Idiopathic generalized epilepsies (IGEs) may start in infancy, childhood, or adolescence, but some have an onset in adulthood. They are genetically determined and affect otherwise healthy people of both sexes and all races, and are generally lifelong. Some, however, are age related. IGEs account for nearly a third of all epilepsies.
Roberto H, Caraballo   +1 more
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Photosensitivity in generalized epilepsies

Epilepsy & Behavior, 2017
Photosensitivity, which is the hallmark of photosensitive epilepsy (PSE), is described as an abnormal EEG response to visual stimuli known as a photoparoxysmal response (PPR). The PPR is a well-recognized phenomenon, occurring in 2-14% of patients with epilepsy but its pathophysiology is not clearly understood.
Shervonne, Poleon, Jerzy P, Szaflarski
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Idiopathic Generalized Epilepsies Imitating Focal Epilepsies

Epilepsia, 2005
Summary:  Classification of epileptic seizures and epilepsy syndromes as either focal or generalized is a fundamental and early part in the diagnostic process and is generally fairly easily accomplished. However, in patients with idiopathic generalized epilepsies, seizure and EEG features may suggest, particularly to the unwary, the occurrence of focal
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GENERALIZED HYPERHIDROSIS FOLLOWING EPILEPSY

British Journal of Dermatology, 1971
SUMMARY.— A case is reported of the sudden development in an elderly woman of severe generalized hyperhidrosis, precipitated by heat, emotion and the ingestion of warm drinks. The abnormal sweating followed within a few days of the onset of epilepsy, and it is suggested that the hyperhidrosis may have followed a small cerebrovascular accident in the ...
W J, Cunliffe, C E, Johnson, J L, Burton
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