肌阵挛发作

肌阵挛发作

1

[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。

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 .
2

肌阵挛发作起病年龄（13.1±3.4）岁；

Myoclonic seizures began at age of ( 13.1 ± 3.4 ) years .
3

Ⅰ型主要表现为继发性不典型失神和负性肌阵挛发作，神经心理损伤预后不良；

Type ⅰ primarily represents ⅱ secondary atypical absences and negative myoclonus , often with poor neuropsychologic prognosis .
4

癫痫发作类型，全身性强直阵挛发作4例，肌阵挛发作1例，复杂部分性发作4例，简单部分性发作3例。

And according to the seizure types of epilepsy , they included : 4 cases of generalized tonic clonic seizure , 1 case of clonic seizure , 4 cases of complex partial seizures , 3 cases of simple partial seizure .