Mahant Neil, Cordato Dennis J, Fung Victor S C
Department of Neurology, Westmead Hospital, Westmead New South Wales, Australia.
Mov Disord. 2003 Apr;18(4):452-5. doi: 10.1002/mds.10382.
We report on a patient with spontaneous and stimulus-sensitive myoclonic jerks and dystonia of the right leg that had been present since infancy. Magnetic resonance imaging showed a linear area of gliosis confined to the left posterolateral putamen. This is the first report of focal myoclonus-dystonia of the lower limb secondary to a putaminal lesion.
我们报告一例自婴儿期起就出现自发性及刺激敏感性肌阵挛性抽搐和右腿肌张力障碍的患者。磁共振成像显示胶质增生的线性区域局限于左侧后外侧壳核。这是首例关于继发于壳核病变的下肢局灶性肌阵挛-肌张力障碍的报告。