Extensive organic lesion of the temporal lobes

Neurological status. The results of the clinical examination depend on the etiology of CE. With extensive organic lesion of the temporal lobes (porecephalic cysts, tumors), contralateral symptoms of prolapse (hemiparesis) may appear. Often, microfocal symptoms

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Neurological status. The results of the clinical examination depend on the etiology of CE. With extensive organic lesion of the temporal lobes (porecephalic cysts, tumors), contralateral symptoms of prolapse (hemiparesis) may appear. Often, microfocal symptoms

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Simple partial seizures

Simple partial seizures often precede complex partial seizures, as well as seizures with secondary generalization. The main criterion of simple partial seizures is the safety of consciousness during paroxysms, which manifest as motor, sensory, autonomic-visceral,

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Simple partial seizures often precede complex partial seizures, as well as seizures with secondary generalization. The main criterion of simple partial seizures is the safety of consciousness during paroxysms, which manifest as motor, sensory, autonomic-visceral,

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Temporal epilepsy (VE)

VE is a localized, often symptomatic form of epilepsy, in which the epileptogenic focus is localized in the temporal lobe. Hughlings Jackson, apparently, was the first who in 1889 associated the occurrence of certain attacks

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VE is a localized, often symptomatic form of epilepsy, in which the epileptogenic focus is localized in the temporal lobe. Hughlings Jackson, apparently, was the first who in 1889 associated the occurrence of certain attacks

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Juvenile myoclonic epilepsy (UME) (Egg syndrome).

Juvenile myoclonic epilepsy is a form of idiopathic generalized epilepsy of adolescence with an identified genetic defect, which is characterized by massive bilateral myoclonic seizures that occur predominantly in the hands during the period after

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Juvenile myoclonic epilepsy is a form of idiopathic generalized epilepsy of adolescence with an identified genetic defect, which is characterized by massive bilateral myoclonic seizures that occur predominantly in the hands during the period after

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Epilepsy with myoclonic absans (EMA) – Tassinari syndrome

Epilepsy with myoclonic absences (EMA) – Tassinari syndrome is a rare form of absence epilepsy, which is characterized by attacks of absences accompanied by massive muscle myoclonia of the shoulder girdle and hands. In the

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Epilepsy with myoclonic absences (EMA) – Tassinari syndrome is a rare form of absence epilepsy, which is characterized by attacks of absences accompanied by massive muscle myoclonia of the shoulder girdle and hands. In the

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Century myoclonus with absences (Jevons syndrome)

Century myoclonus with absences (Jevons syndrome) (MVA) is a form of abscess epilepsy, characterized by short absence with myoclonia of the eyelids, setting up the eyeballs, expressed photo-sensitivity. This syndrome was first described by Jeavons

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Century myoclonus with absences (Jevons syndrome) (MVA) is a form of abscess epilepsy, characterized by short absence with myoclonia of the eyelids, setting up the eyeballs, expressed photo-sensitivity. This syndrome was first described by Jeavons

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