Year: 2019

One of the first definitions of epileptic status was given in 1904 by Clark and Pront: “ES is a condition in which seizures recur with such frequency that coma and exhaustion are constant between them.”

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

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.

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

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

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.

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

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,

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

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