Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research 5-том 2-сан (2024)
MODERN VIEWS ON JUVENILE MYOCLONIC EPILEPSY
Абдурахманова Манзура Абдумуталовна, Туйчибаева Нодира Мираталиевна
Аннотация
Juvenile myoclonic epilepsy (JME) is a common idiopathic epilepsy, accounting for 10% of all epilepsies. It is characterized as a syndrome of generalized genetic epilepsy with a peak development at the age of 12-18 years. The disease was initially thought to have a benign lifelong course due to normal intelligence and positive response to antiepileptic drugs (AEDs). As a result of new research, juvenile myoclonic epilepsy (JME) is no longer considered a homogeneous disease. However, recent studies indicate that cognitive dysfunction and neuropsychological impairment are a major component of the JME phenotype.
Ювенильная миоклоническая эпилепсия, нейропсихология, когнитивные росстройства, генетическая, электроэнцефалографияJuvenile myoclonic epilepsy, neuropsychology, cognitive disorders, genetic, electroencephalographyЮвенил миоклоник эпилепсия, нейропсихология, когнитив бузилишлар, генетик, эелектроэнцефалография
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