This case represents a novel association of a DNM1 gene mutation with status epilepticus and progressive bilateral mesial temporal sclerosis. This could have future implications for treatment in patients with DNM1 mutation and refractory epilepsy as the mesial temporal sclerosis may become bilateral, making the patient a poor surgical candidate.
|Original language||English (US)|
|Number of pages||3|
|Journal||Clinical Case Reports|
|State||Published - Nov 2018|
All Science Journal Classification (ASJC) codes