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笑性癫痫。发病于新生儿期。

Gelastic Epilepsy. Onset in neonatal period.

作者信息

Sher P K, Brown S B

出版信息

Am J Dis Child. 1976 Oct;130(10):1126-31. doi: 10.1001/archpedi.1976.02120110088013.

DOI:10.1001/archpedi.1976.02120110088013
PMID:973617
Abstract

The phenomenon of gelastic epilepsy was first described in 1873, yet fewer than 100 patients with this disorder have been reported on to date. The purpose of this article is to report on the first two patients to our knowledge with the onset of these seizures in the immediate neonatal period. Both patients have been shown to have posterior hypothalamic mass lesions presumably of congenital origin, and have remained free of neurologic progression of the disease with conservative treatment.

摘要

1873年首次描述了笑性癫痫现象,然而迄今为止报道的患有这种疾病的患者不到100例。本文的目的是报告据我们所知最初两名在新生儿期即刻出现这些发作的患者。两名患者均显示有推测为先天性起源的下丘脑后部肿块病变,并且通过保守治疗疾病未出现神经学进展。

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1
Gelastic Epilepsy. Onset in neonatal period.笑性癫痫。发病于新生儿期。
Am J Dis Child. 1976 Oct;130(10):1126-31. doi: 10.1001/archpedi.1976.02120110088013.
2
Gelastic epilepsy and hypothalamic hamartomas: neuroanatomical analysis of brain lesions in 100 patients.发作性笑性癫痫和下丘脑错构瘤:100 例患者脑损伤的神经解剖学分析。
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Intrinsic epileptogenesis of hypothalamic hamartomas in gelastic epilepsy.笑性癫痫中下丘脑错构瘤的内在癫痫发生机制
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[Gelastic epilepsy and precocious puberty in hamartoma of the hypothalamus].[下丘脑错构瘤中的痴笑性癫痫和性早熟]
Klin Padiatr. 1991 Nov-Dec;203(6):439-47. doi: 10.1055/s-2007-1025470.
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[Hypothalamic hamartoma and gelastic crises. Apropos of 7 cases].
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Seizures presenting as incessant laughter: a case of gelastic epilepsy.以持续性大笑为表现的癫痫发作:一例痴笑性癫痫病例
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Cursive epilepsy and gelastic epilepsy.痴笑性癫痫和 咯咯笑性癫痫。
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Gelastic seizures of neocortical origin confirmed by resective surgery.经切除性手术证实的新皮质起源的痴笑发作
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Intractable gelastic seizures during infancy: ictal positron emission tomography (PET) demonstrating epileptiform activity within the hypothalamic hamartoma.婴儿期难治性痴笑发作:发作期正电子发射断层扫描(PET)显示下丘脑错构瘤内的癫痫样活动。
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Endoscopic endonasal resection of olfactory tract hamartoma for pediatric epilepsy.内镜经鼻内嗅束脑回造瘘术治疗小儿癫痫的嗅沟脑膜瘤。
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2
Pure endoscopic management of epileptogenic hypothalamic hamartomas.癫痫源性下丘脑错构瘤的纯内镜治疗
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Dacrystic seizures: demographic, semiologic, and etiologic insights from a multicenter study in long-term video-EEG monitoring units.
流泪性发作:来自长期视频脑电图监测单元的多中心研究中的人口统计学、半影学和病因学见解。
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A review on the management of epilepsy associated with hypothalamic hamartomas.下丘脑错构瘤相关癫痫的治疗综述
Childs Nerv Syst. 2009 Apr;25(4):423-32. doi: 10.1007/s00381-008-0798-y. Epub 2009 Jan 20.
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Symmetric ganglionic hamartoma of hypothalamus appearing as four "mamillary" bodies.表现为四个“乳头体”的下丘脑对称性神经节错构瘤。
Acta Neuropathol. 1982;56(3):238-40. doi: 10.1007/BF00690641.
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Epileptic laughter with precocious puberty.伴有性早熟的癫痫性发笑。
Arch Dis Child. 1978 Dec;53(12):965-6. doi: 10.1136/adc.53.12.965.
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Epileptic laughter: electroclinical and cinefilm report of a case.癫痫性发笑:一例患者的临床电生理及电影记录报告
J Neurol. 1979 May 2;220(3):215-22. doi: 10.1007/BF00705539.