MODERN VIEWS ON JUVENILE MYOCLONIC EPILEPSY

Абдурахманова Манзура Абдумуталовна, Туйчибаева Нодира Мираталиевна

Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research · 2024-yil

Annotatsiya

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.

Maqola ma’lumotlari
MualliflarАбдурахманова Манзура Абдумуталовна, Туйчибаева Нодира Мираталиевна
JurnalЖурнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research
Nashr sanasi2024-05-27
Jild5
Son2
TilRus

Kalit so‘zlar

Ювенильная миоклоническая эпилепсия, нейропсихология, когнитивные росстройства, генетическая, электроэнцефалография, Juvenile myoclonic epilepsy, neuropsychology, cognitive disorders, genetic, electroencephalography, Ювенил миоклоник эпилепсия, нейропсихология, когнитив бузилишлар, генетик, эелектроэнцефалография

Ilmiy soha

Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research jurnalidan boshqa maqolalar

Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research — barcha maqolalar