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.
| Mualliflar | Абдурахманова Манзура Абдумуталовна, Туйчибаева Нодира Мираталиевна |
|---|---|
| Jurnal | Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research |
| Nashr sanasi | 2024-05-27 |
| Jild | 5 |
| Son | 2 |
| Til | Rus |
Ювенильная миоклоническая эпилепсия, нейропсихология, когнитивные росстройства, генетическая, электроэнцефалография, Juvenile myoclonic epilepsy, neuropsychology, cognitive disorders, genetic, electroencephalography, Ювенил миоклоник эпилепсия, нейропсихология, когнитив бузилишлар, генетик, эелектроэнцефалография
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