Kozhevnikov syndrome (epilesia partialis continua) CK

The disease was first described by A.Ya. Kozhevnikov in 1895. In the original description, it is noted that epilesia partialis continua is characterized by a combination of frequent, almost constant motor Jackson paroxysms with local

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The disease was first described by A.Ya. Kozhevnikov in 1895. In the original description, it is noted that epilesia partialis continua is characterized by a combination of frequent, almost constant motor Jackson paroxysms with local

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Lennox-Gasto Syndrome (SLG)

SLH refers to generalized symptomatic epileptic syndromes and is characterized by a combination of several types of generalized seizures, a special type of high-amplitude EEG (gypsarhythmia), and mental and motor developmental delay. According to S.

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SLH refers to generalized symptomatic epileptic syndromes and is characterized by a combination of several types of generalized seizures, a special type of high-amplitude EEG (gypsarhythmia), and mental and motor developmental delay. According to S.

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Rolandic epilepsy

Rolandic epilepsy (RE) – benign partial epilepsy of childhood with centro-temporal adhesions ER – nosologically independent form of idiopathic partial epilepsy. It is characterized by: · Debut in 3-13 years; · Simple partial motor paroxysms

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Rolandic epilepsy (RE) – benign partial epilepsy of childhood with centro-temporal adhesions ER – nosologically independent form of idiopathic partial epilepsy. It is characterized by: · Debut in 3-13 years; · Simple partial motor paroxysms

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Psychomotor frontal attacks

Psychomotor frontal attacks are accompanied by impaired consciousness, gaze stopping, bilateral tonic tension of the hands, gestural automatism, pedaling, vocalization, tonic turning of the eyes and head. Possible secondary generalization. The above types of frontal

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Psychomotor frontal attacks are accompanied by impaired consciousness, gaze stopping, bilateral tonic tension of the hands, gestural automatism, pedaling, vocalization, tonic turning of the eyes and head. Possible secondary generalization. The above types of frontal

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Frontal Epilepsy (PE)

PEs are ranked second in frequency of occurrence among partial epilepsy (20–30% Manford, 1995). Etiology. Etiological factors determining the development of PE include traumatic brain injury, tumors, birth trauma, brain dysgenesis, neuroinfection, etc. (Rasmussen,Ush). Clinic.

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PEs are ranked second in frequency of occurrence among partial epilepsy (20–30% Manford, 1995). Etiology. Etiological factors determining the development of PE include traumatic brain injury, tumors, birth trauma, brain dysgenesis, neuroinfection, etc. (Rasmussen,Ush). Clinic.

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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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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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