Kanmaz Seda, Özcan Muhittin, Şimşek Erdem, Serin Hepsen M, Aydogdu İbrahim, Gökben Sarenur, Tekgül Hasan
Department of Pediatrics, Division of Child Neurology, Ege University Medical Faculty, Izmir, Turkey.
Department of Pediatrics, Ege University Medical Faculty, Izmir, Turkey.
J Pediatr Neurosci. 2020 Apr-Jun;15(2):153-156. doi: 10.4103/jpn.JPN_128_19. Epub 2020 Jun 27.
Isaacs syndrome is rare disorder with peripheral nerve hyperexcitability syndromes with acquired neuromyotonia in childhood. We present a 13-year-old girl with muscle stiffness and neuromyotonia diagnosed Isaac syndrome with spontaneous discharge potentials on motor unit in electromyography and the diagnosis supported by the presence of antinuclear antibodies. A successful treatment was obtained using low-dose carbamazepine. Cause of Isaacs syndrome is unknown, generally thought to be an autoimmune etiology with voltage-gated potassium channelopathy; it sometimes occurs as a paraneoplastic syndrome. Early use of electromyography has critical role in the differential diagnosis with certain muscle disorders and peripheral nerve hyperexcitability syndromes.
艾萨克斯综合征是一种罕见的疾病,属于儿童期获得性神经性肌强直的周围神经兴奋性增高综合征。我们报告一名13岁女孩,她患有肌肉僵硬和神经性肌强直,经肌电图检查发现运动单位有自发放电电位,确诊为艾萨克斯综合征,且抗核抗体的存在支持了这一诊断。使用低剂量卡马西平治疗取得了成功。艾萨克斯综合征的病因尚不清楚,一般认为是自身免疫性病因伴电压门控钾通道病;它有时作为副肿瘤综合征出现。早期使用肌电图在与某些肌肉疾病和周围神经兴奋性增高综合征的鉴别诊断中起关键作用。