Spitz M C, Jankovic J, Killian J M
Neurology. 1985 Mar;35(3):366-70. doi: 10.1212/wnl.35.3.366.
We report two brothers who were of consanguineous parents and who displayed a unique association of motor and vocal tics, parkinsonism, distal muscular atrophy, and acanthocytosis. In the older brother, leg weakness and muscle wasting started at age 13, and he became wheelchair bound at 40. Electrophysiologic studies and muscle biopsy confirmed diffuse denervation. Involuntary vocalizations and facial tics began at age 36, but within 5 years the tics were replaced by progressive parkinsonism with supranuclear ophthalmoparesis. CSF studies implied impaired central dopamine and serotonin turnover. In the younger brother, orofacial tics started at age 36, vocalizations and fasciculations in the legs began 1 year later, and parkinsonian findings were present at age 40. This is the first report of an association of Tourettism, parkinsonism, motor neuron disease, and acanthocytosis occurring as an autosomal recessive syndrome.
我们报告了一对父母为近亲的兄弟,他们表现出运动和发声抽动、帕金森症、远端肌肉萎缩和棘红细胞增多症的独特组合。哥哥13岁时开始出现腿部无力和肌肉萎缩,40岁时只能依靠轮椅行动。电生理研究和肌肉活检证实存在弥漫性神经失用。36岁时开始出现不自主发声和面部抽动,但5年内抽动被进行性帕金森症伴核上性眼肌麻痹所取代。脑脊液研究提示中枢多巴胺和血清素代谢受损。弟弟36岁时开始出现口面部抽动,1年后腿部出现发声和肌束震颤,40岁时出现帕金森症表现。这是首例作为常染色体隐性综合征出现的抽动秽语综合征、帕金森症、运动神经元病和棘红细胞增多症关联的报告。