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The Causes of Epilepsy最新文献

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Genetic Epilepsy with Febrile Seizures Plus (GEFS+) 遗传性癫痫伴热性发作+ (GEFS+)
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.020
Genetic epilepsy with febrile seizures plus (GEFS+) is a spectrum of seizure disorders of varying severity. GEFS+ is usually diagnosed in families whose members have a combination of febrile seizures, which are triggered by a high fever, and recurrent seizures (epilepsy) of other types, including seizures that are not related to fevers (afebrile seizures). The additional seizure types usually involve both sides of the brain (generalized seizures); however, seizures that involve only one side of the brain (partial seizures) occur in some affected individuals. The most common types of seizure in people with GEFS+ include myoclonic seizures, which cause involuntary muscle twitches; atonic seizures, which involve sudden episodes of weak muscle tone; and absence seizures, which cause loss of consciousness for short periods that appear as staring spells.
遗传性癫痫伴发热性癫痫发作(GEFS+)是一系列严重程度不同的癫痫发作障碍。GEFS+通常在成员有发热性癫痫发作(由高热引发)和其他类型的反复发作(癫痫),包括与发热无关的癫痫发作(发热性癫痫发作)的组合的家庭中被诊断出来。额外的癫痫类型通常涉及大脑两侧(全身性癫痫发作);然而,癫痫发作只涉及大脑的一侧(部分癫痫发作)发生在一些受影响的个体。GEFS+患者最常见的癫痫发作类型包括肌阵挛性发作,引起不自主肌肉抽搐;失张力性癫痫,包括肌肉张力的突然发作;以及失神发作,会导致短暂的意识丧失,表现为凝视。
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引用次数: 0
Epilepsy Associated with Alzheimer’s Disease and Other Adult Neurodegenrative Disorders 癫痫与阿尔茨海默病和其他成人神经退行性疾病相关
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.108
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引用次数: 0
Epilepsy Associated with Subarachnoid Hemorrhage 癫痫伴蛛网膜下腔出血
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.095
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引用次数: 0
PCDH19 Mutations Related Epilepsy: Phenotype and Genotype PCDH19突变与癫痫相关:表型和基因型
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.024
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引用次数: 0
Neuronal Ceroid Lipofuscinoses 神经元类脂褐细胞病
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.051
Ceroid Lipofuscinoses
neurodegenerative disorders of childhood, with an incidence of about 1 in 25,000 births. Several subtypes of the disease are classified on the basis of age of onset, clinical features, biochemical analysis and detailed pathological examination of patient tissue with electron microscopy. NCLs are characterized by progressive motor and cognitive deterioration, seizures, early death, and often visual loss. NEURONAL CEROID LIPOFUSCINOSES
儿童神经退行性疾病,发病率约为1 / 25,000。根据发病年龄、临床特征、生化分析和患者组织电镜详细病理检查,将本病分为几种亚型。ncl的特点是进行性运动和认知功能减退、癫痫发作、早期死亡,并经常出现视力丧失。神经元类脂褐变
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引用次数: 0
Approach to the Diagnosis of Epilepsy Presenting with Myoclonus 以肌阵挛为表现的癫痫的诊断探讨
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.013
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引用次数: 0
Startle-Induced and Other Sensory-Induced Epilepsy 惊吓性和其他感觉性癫痫
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.120
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引用次数: 0
Familial Focal Epilepsy with Variable Foci 变焦的家族性局灶性癫痫
Pub Date : 2019-04-30 DOI: 10.1007/978-1-84882-128-6_169
Xue-feng Wang, F. Xiao
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引用次数: 3
Dentatorubral-Pallidoluysian Atrophy; DRPLA
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.048
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引用次数: 0
Seizures Induced by Eating, a Rare but Special Form of Reflex Epilepsy 进食引起的癫痫,一种罕见但特殊的反射性癫痫
Pub Date : 2019-04-30 DOI: 10.1017/9781108355209.123
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引用次数: 0
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The Causes of Epilepsy
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