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Follow-up study of idiopathic generalized epilepsy with associated absence seizure and myoclonic epilepsy of infancy

机译:特发性通用癫痫的随访研究与婴儿疾病癫痫发作和肌阵挛性癫痫发作

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Highlights ? Myoclonic seizures and absence seizures are rarely associated in Myoclonic epilepsy of infancy. ? IGE children featuring MEI associated with absence seizures have an excellent prognosis and seizure outcome. ? The electroclinical features of this group were equivalent to myoclonic epilepsy of infancy. Abstract We evaluated the long-term prognosis of patients featuring the association of absence s and myoclonic epilepsy of infancy. Our cohort consisted of 10 male subjects with mean age at seizure onset of 29 months. Follow-up data included seizure outcome and EEG findings. All individuals received antiepileptic drugs (AEDs) as monotherapy (6 patients) or polytherapy (4 patients) for a mean period of 24 months. Over a 30–60 month evaluation period (mean: 43 months), all patients were seizure-free. Follow-up data after withdrawal of antiepileptic therapy were obtained for a mean period of 22 months. None of the children did develop other age-related epileptic syndrome after AEDs discontinuation. Furthermore, follow-up EEG data after drugs withdrawal were normal and none of the patients showed cognitive impairment. In conclusion, we confirm that absence seizures may occur in association with myoclonic epilepsy of infancy. This condition shows excellent prognosis with either favourable neurologic development and seizure outcome in these children.
机译:强调 ?肌阵挛性癫痫发作和缺乏癫痫发作很少在婴儿的肌阵挛性癫痫中有关。还IgE儿童具有与缺失癫痫发作相关的MEI具有优异的预后和癫痫发作结果。还该组的电灭菌特征与初期肌肌肺癫痫相同。摘要我们评估了具有缺失的缺失和初期鼻窦癫痫患者的患者的长期预后。我们的队列由10名男性受试者组成,癫痫发作为29个月的平均年龄。随访数据包括癫痫发作结果和EEG调查结果。所有个人都接受了抗癫痫药物(AEDs)作为单药治疗(6名患者)或聚类治疗(4名患者)24个月。超过30-60个月的评估期(平均:43个月),所有患者都被扣押。获得抗癫痫疗法后的后续数据,均为平均22个月。在停药后,没有孩子患有其他与年龄相关的癫痫症综合征。此外,药物戒断后的随访脑电图数据正常,患者没有任何患者表现出认知障碍。总之,我们确认缺失癫痫发作与婴儿症的肌阵挛性癫痫有关。这种情况表明,具有良好的预后,具有良好的神经系统发育和这些儿童的癫痫发作结果。

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