Juvenile myoclonic epilepsy. Epilepsy with impulsive petit mal.
Juvenile myoclonic epilepsy. Epilepsy with impulsive petit mal.
复制标题
青少年肌阵挛性癫痫。
DOI：
--
复制
发表时间：
1989
影响因子：
6.1
通讯作者：
Dieter Janz
中科院分区：
文献类型：
--
作者：
Dieter Janz
与第一位已知患有婴儿痉挛症的患者一样，第一位众所周知的青少年肌阵挛性癫痫 (JME) 患者也是一位医生的儿子。 Herpin 是关于这种情况的经典报告的作者，他试图用各种术语来界定主要症状，例如“冲动”、“sécousses”、“癫痫骚动”，而不附加任何标签（表 J）。拉伯特后来将中性但富有表现力的描述“肌阵挛”引入癫痫术语中。为了防止与罕见的进行性退行性肌阵挛癫痫混淆，伦德堡在他的术语中强调了抽动的间歇性本质。 1957年，克里斯蒂安和作者根据47例病例，将这种以间歇性早晨抽搐为特征的特发性癫痫描述为一种临床上可明确定义的癫痫综合征。近三十年后，这种综合症在美国被重新发现，并由 Asconapé 和 Penry、Delgado-Escueta 和 Enrile-Bacsal 引起英语世界的注意。德尔加多·埃斯库塔（Delgado-Escueta），在他之前，马蒂斯以他的名字命名了这种综合症，以此向这位作家表示敬意。
LIKE the first patient known to have infantile spasms, the first patient with juvenile myoclonic epilepsy (JME) whose history was well known was a doctor's son. Herpin, author of the classical report on this condition, attempted to circumscribe the principal symptom with various terms, such as "impulsions," "sécousses," "commotions épileptiques," without attaching any labels to it (Table J). Rabot later introduced the neutral yet expressive description "myoclonia" into the terminology of epilepsy. In order to prevent confusion with the rare, progressively degenerative myoclonus epilepsy, Lundborg in his terminology emphasized the intermittent nature of the jerks. In 1957, Christian and the writer described this type of idiopathic epilepsy, characterized by intermittent morning jerks, on the basis of 47 cases as a clinically and clearly definable epileptic syndrome. Almost thirty years later, this syndrome has been rediscovered in the United States and brought to the notice of the English-speaking world by Asconapé and Penry and by Delgado-Escueta and Enrile-Bacsal. Delgado-Escueta, and before him, Matthes honored the writer by naming the syndrome after him.