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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