Roubergue A, Beauvais P, Richardet J M
Arch Fr Pediatr. 1985 May;42(5):377-8.
A new case of Bobble-head doll syndrome with aqueductal stenosis is presented in a 14 year-old boy. Ventriculocisternostomy performed 8 years after the onset of the abnormal movement resulted in moderate reduction of the head bobbling. Twenty-two cases were found in a review of the literature. In all cases there was a chronic slowly progressive hydrocephalus with usually a cyst of the third ventricle; aqueductal stenosis was less frequent. When recorded, psychomotor development was impaired. Treatment is neurosurgical. Pathogenesis remains unknown.
本文报告了一名14岁男孩患有的摆动性头部痉挛综合征合并导水管狭窄的新病例。在异常运动发作8年后进行了脑室腹腔分流术，头部摆动症状得到了适度缓解。通过文献回顾发现了22例相关病例。所有病例均存在慢性进行性脑积水，通常伴有第三脑室囊肿；导水管狭窄相对少见。据记录，患者的精神运动发育均有受损。治疗方法为神经外科手术。其发病机制尚不清楚。
