Atypical course of severe myoclonic epilepsy of infancy (Dravet syndrome)
A clinical observation of a patient with Dravet syndrome caused by SCN1A gene mutation is presented. Dravet syndrome is a severe epileptic encephalopathy that occurs in early childhood, accompanied by seizure polymorphism, drug-resistant course and severe cognitive impairment. The current clinical...
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| Main Authors: | , , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
IRBIS LLC
2024-07-01
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| Series: | Эпилепсия и пароксизмальные состояния |
| Subjects: | |
| Online Access: | https://www.epilepsia.su/jour/article/view/1043 |
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