Vieira J B, Rosa E D
Arq Neuropsiquiatr. 1985 Jun;43(2):194-7. doi: 10.1590/s0004-282x1985000200011.
Case report of a 9 years old boy with Kinsbourne's syndrome. This condition was characterized by the subacute onset of polymyoclonia, cerebellar ataxia and opsoclonus that set later, following an herpes zoster infection. Steroid therapy resulted in rapid dramatic improvement of neurological symptoms.
一名9岁患有金氏综合征男孩的病例报告。该病症的特征为多肌阵挛、小脑共济失调和眼球阵挛的亚急性发作，这些症状在带状疱疹感染后较晚出现。类固醇治疗使神经症状迅速显著改善。
