用 Y—氨基丁酸(GABA)治疗遗传性共济失调获显效者文献报道尚少,笔者曾治疗一例 Marie 氏共济失调患者,疗效显著,现报告如下。患者,男,38岁,农民,患者于1986年6月始感走路不稳,并进行性加重,尤以夜间明显。一年后出现走路易摔倒,语音不利落,轻微头晕,双手笨拙,无阳萎及猝倒史。二便正常。有家族史(见家系谱)。 Y-aminobutyric acid (GABA) treatment of hereditary ataxia was markedly reported in the literature is still small, I had treatment of a case of Marie’s ataxia patients with significant effect, are as follows. Patient, male, 38 years old, peasant, patient Initially unstable and aggravating in June 1986, especially at night. A year later, he fell prone to walk, his voice was not conducive to falling, slightly dizzy, his hands clumsy, and had no history of impotence and catching up. Two will be normal. Family history (see pedigree).