Braakman Hilde M, Verhoeven Judith S, Erasmus Corrie E, Haaxma Charlotte A, Willemsen Marjolein H, Schelhaas H Jurgen
Department of Neurology Academic Center for Epileptology Kempenhaeghe and Maastricht UMC+Heeze the Netherlands.
Department of Neurology Radboud University Medical Center Nijmegen the Netherlands.
Epilepsia Open. 2017 May 16;2(3):343-344. doi: 10.1002/epi4.12059. eCollection 2017 Sep.
encodes Nav1.6, one of the main voltage-gated sodium channel subunits in the brain, and mutations lead to epileptic encephalopathy. Particular mutations render the mutant channel more susceptible to inhibition by phenytoin. Yet, the potentially severe side effects of phenytoin maintenance therapy, especially cognitive impairment, are undesirable in these already cognitively impaired patients. We describe a 5-year-old patient with encephalopathy in whom phenytoin proved successful as emergency treatment to prevent clustering of seizures and status epilepticus, thus hospital stays. The ketogenic diet, levetiracetam, zonisamide, topiramate, and phenytoin maintenance therapy resulted in adverse reactions not previously documented in encephalopathy.
编码Nav1.6,它是大脑中主要的电压门控钠通道亚基之一,突变会导致癫痫性脑病。特定的突变使突变通道更容易受到苯妥英钠的抑制。然而,苯妥英钠维持治疗潜在的严重副作用,尤其是认知障碍,在这些已经存在认知障碍的患者中是不可取的。我们描述了一名5岁的脑病患者,苯妥英钠作为紧急治疗成功地预防了癫痫发作的聚集和癫痫持续状态,从而缩短了住院时间。生酮饮食、左乙拉西坦、唑尼沙胺、托吡酯和苯妥英钠维持治疗导致了脑病患者以前未记录的不良反应。