进行性肌阵挛性癫痫又称Lundborg—Unverricht综合征,是一种少见的家族遗传性疾病。1891年Unverricht首先描述。国内报道甚少。我科最近收治同一家族的二个病例,现报告如下。临床资料例1,男,17岁,1986年9月30日入院。患者于13岁时开始出现双下肢闪动性抽动,每日5～6 Progressive myoclonic epilepsy, also known as Lundborg-Unverricht syndrome, is a rare family genetic disease. Unverricht first described in 1891. Domestic reports rarely. Our department recently admitted two cases of the same family, are as follows. Clinical data example 1, male, 17 years old, September 30, 1986 admission. Patients start flashing both lower extremities at the age of 13, 5-6 per day