Abstract

Dravet syndrome is severe form of epilepsy in early childhood, characterized by drug-resistant course and seizures polymorphism. The article describes clinical case of 2-year remission in a child by anticonvulsant polytherapy combined with diacomit followed by gradual withdrawal of several anticonvulsants. This case confirms reasonability of aggressive therapy at an initial treatment stage in order to improve its prognosis and cognitive decline limitation.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call