myoclonic
英
美
网络 肌阵挛的; 肌阵挛; 肌阵挛性; 发作之肌肉抽动
双语例句
- Juvenile myoclonic epilepsy is an idiopathic generalized epileptic syndrome characterized by myoclonic jerks, generalized tonic-clonic seizures, and sometimes absence seizures.
青少年肌阵挛性癫是一种以晨起肌阵挛、全身强直-阵挛发作为临床特征的特发性全身性癫综合征，有时伴有失神发作。 - The patient demonstrates changes in personality, behavior, and memory, followed by myoclonic jerks, blindness, and spasticity.
病人先表现为人格，行为和记忆力的变化，然后出现痉挛性的反射，失明及强直状态。 - Results The clinical signs of these two cases included dementia, myoclonic, motor dysfunction, behavior abnormalities and extrapyramidal signs.
结果患者临床表现为智能障碍、肌阵挛、运动障碍、行为异常及锥体外系症状。 - Visual and cerebellar signs appeared comparatively early besides mental and myoclonic changes, but signs of pyramidal damage were not obvious relatively.
除痴呆和肌阵挛表现明显外，视力损伤和小脑征出现相对较早，而锥体束损害相对不太明显； - Objective To study the characteristics of molecular genetics concerning Chinese myoclonic epilepsy and ragged-red fiber disease ( MERRF).
目的探讨肌阵挛癫痫伴破碎红纤维综合征（MERRF）的分子遗传学特点。 - Myoclonic seizures began at age of ( 13.1 ± 3.4) years.
肌阵挛发作起病年龄（13.1±3.4）岁； - This paper retrospectively analyzed the clinical data of 31 survivors from three families with benign adult familial myoclonic epilepsy ( BAFME).
对三个良性家族性肌阵挛癫痫（BAFME）家系中的31例存活患者的临床资料进行回顾性分析。 - Epilepsy with myoclonic absences
肌阵挛失神性癫痫 - Clinical characteristics of benign adult familial myoclonic epilepsy in three families
良性成人家族性肌阵挛癫痫三家系临床特点分析 - The diagnosis of myoclonic SE and nonconvulsive SE might be difficult and Video-EEG monitoring should be performed.
肌阵挛性SE、非惊厥性SE临床诊断困难，应行Video-EEG监测； - Effects of sleep deprivation on cortical excitability in patients affected by juvenile myoclonic epilepsy: A combined transcranial magnetic stimulation and EEG study
睡眠剥夺对青少年肌阵挛性癫痫患者皮质兴奋性的影响：经颅磁刺激和EEG的联合研究 - Methods The clinical data, interictal, ictal and sleep EEG of a case of epilepsy with myoclonic absences were studied and followed-up.
方法对1例肌阵挛失神性癫痫患者的临床表现、发作间期、发作期及睡眠脑电图监测结果进行研究和随访。 - Nine families in this study, the major clinical phenotype was FS and FS+ also includes a small number of FS+ and absence seizures, FS+ with myoclonic seizures, FS+ with focal seizures and idiopathic generalized epilepsy.
[结论]1.本文收集的9个家系中，其临床表型以FS、FS+为主要类型，还包括少数FS+伴失神发作、FS+伴肌阵挛发作、FS+伴局灶性发作以及特发性全面性癫痫。