Rolandic Epilepsy: Self-Limited Epilepsy with Centrotemporal Spikes

Author:

Guliyeva Ulviyya,Nino Tatishvili Nana,Kaiyrzhanov Rauan

Abstract

Childhood epilepsy with centrotemporal spikes, had been previously considered as benign childhood epilepsy. According to the new classification proposed by Sheffer I. and colleagues the term “benign” has been changed to “self-limited”. Many studies reported that BECTS may cause transient or long lasting cognitive and behavioral disturbances. Rolandic epilepsy is the most frequent among the childhood focal epilepsy and may account for about 15–25% of all epileptic syndromes diagnosed between the ages of 5 to 15 years. The incidence range changes between 7.1–21 per 100000 in population younger than 15 years with male predominance. The age of onset in 90% of cases between 1 and 10 years with peak around 6–7 years. Seizures mainly occur during a night sleep, whereas the probability of awake seizures are less than 10%. The characteristic clinical features are: (1) focal motor seizure with unilateral orofacial tonic or clonic contractions; (2) speech arrest; (3) hypersalivation; (4) sensory symptoms represented by unilateral numbness or paresthesia of tongue, lips, gum and inner part of the check; (5) unilateral clonic jerk in leg and arm with postictal paresis; (6) generalized seizures. The EEG picture is distinctive in Rolandic epilepsy. The background activity is almost always preserved in awake state and during a sleep. The typical interictal EEG pattern is high voltage, diphasic spikes or sharp waves frequently with slow activity on central-midtemporal region. The centrotemporal spikes or rolandic spikes come from the lower rolandic region created a horizontal dipole with maximal electronegativity in the centrotemporal region and electropositivity in the frontal region usually seen unilateral or bilateral. In most cases children with RE have a good prognosis regarding both seizures and neurodevelopment. The remission of seizures usually occurs before the age of 18 years. The cognitive and behavior problem may happen in active period of disease which are reversable in most of patients.

Publisher

IntechOpen

Reference169 articles.

1. Hauser WA, Annegers JF, Kurland LT. Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984. Epilepsia. 1993 May-Jun;34(3):453-468. doi: 10.1111/j.1528-1157.1993.tb02586.x. PMID: 8504780

2. Federico Vigevano, Nicola Specchio, Natalio Fejerman, Chapter 61 - Idiopathic focal epilepsies, Editor(s): Olivier Dulac, Maryse Lassonde, Harvey B. Sarnat, Handbook of Clinical Neurology, Elsevier, Volume 111, 2013,p. 591-604

3. Koutroumanidis M, Panayiotopoulos CP. Benign childhood seizure susceptibility syndromes. In: Rugg-Gunn RJ, Smalls JE, editors. From channels to commissioning – a practical guide to epilepsy. London: International League Against Epilepsy (UK Chapter) and Epilepsy Society; 2015. p. 89-113

4. Chrysostomos P. Panayiotopoulos, Michelle Bureau Roberto H. Caraballo, Bernardo Dalla Bernardina, Thalia Valeta. Idiopathic childhood focal epilepsies. In: Michelle Bureau, Pierre Genton, Charlotte Dravet, Antonio, Delgado-Escueta, Carlo Alberto Tas sinari, Pierre Thomas, Peter Wolf, Epileptic Syndromes in Infancy, Childhood and Adolescence – 5th updated edition, JOHN LIBBEY EUROTEXT,2012. p. 217-224

5. Panayiotopoulos CP. Benign childhood partial epilepsies: benign childhood seizure susceptibility syndromes. J Neurol Neurosurg Psychiatry. 1993 Jan;56(1):2-5. doi: 10.1136/jnnp.56.1.2. PMID: 8429319; PMCID: PMC1014755

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3