myoclonic

myoclonic

美 　英

• 網絡肌躍性；肌陣攣性；發作之肌肉抽動

例句

Myoclonic epilepsy is a genetic disease often can be a family history.

肌陣攣癲癇常為一種遺傳性疾病，可有家族遺傳史。

type of myoclonus status epilepticus: a recurrent myoclonic long hair as the feature.

肌陣攣型癲癇持續狀態：以長時間的反復肌陣攣發作為特征。

there is a specific period in infancy of severe myoclonic seizures, infantile spasms are called.

在嬰兒時期有一種特有的嚴重的肌陣攣發作，被稱之為嬰兒痙攣癥。

Myoclonic seizures have a significant resistance, about 60% of patients satisfied with the efficacy of drug treatment available.

肌陣攣發作具有明顯的抗藥性，約有60%的患者藥物治療可獲得滿意的療效。

Diagnoses were either juvenile myoclonic epilepsy (93. 4%) or juvenile absence epilepsy (6. 6%).

病人診斷分別為青年型肌陣攣性癲癇（93.4%）和少年型失神性癲癇（6.6%）。

Objective To study the clinical features and main factors responsible for diagnostic errors in juvenile myoclonic epilepsy (JME).

目的研究青少年肌陣攣性癲癇（JME）的臨床特點及導致誤診的主要原因。

myoclonic, generalized tonic-clonic seizure and complex partial seizure in 1 each;

單純肌陣攣發作、強直陣攣發作和復雜部分性發作各1例；

Severe myoclonic epilepsy in infants, SME,

又稱嬰兒嚴重肌陣攣性癲癇，

Features of clinical and therapy in juvenile myoclonic epilepsy: an analysis of 87 cases

青少年肌陣攣性癲癎87例臨床及治療特點分析

Results There were 2 patients (6. 3%) only with myoclonic seizure;

結果單純肌陣攣發作2例（6.3%）；