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首页> 外文期刊>Internal medicine. >Stiff-person syndrome associated with cerebellar ataxia and high glutamic acid decarboxylase antibody titer.
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Stiff-person syndrome associated with cerebellar ataxia and high glutamic acid decarboxylase antibody titer.

机译:与小脑性共济失调和高谷氨酸脱羧酶抗体滴度相关的僵人综合征。

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摘要

Glutamic acid decarboxylase (GAD) is the main target of humoral autoimmunity in patients with insulin-dependent diabetes mellitus (IDDM) and stiff-person syndrome. We reviewed the case of a 46-year-old woman who had cerebellar ataxia before getting stiff-person syndrome and IDDM with high anti-GAD autoantibody titers. This was a rare case in which there were both the clinical symptoms of stiff-person syndrome and cerebellar ataxia. In western blot analysis her serum reacted with 65-kDa proteins from rat cerebellum, cerebral cortex, and spinal cord. Autoantibodies to GAD may cause functional impairment of gamma-aminobutyric acid (GABA) neurons in the spinal cord as well as in the cerebellum.
机译:谷氨酸脱羧酶(GAD)是胰岛素依赖型糖尿病(IDDM)和僵人综合征患者的体液自身免疫的主要目标。我们回顾了一个46岁的女性,该女性在获得僵直人综合征和IDDM且抗GAD自身抗体滴度很高之前患有小脑共济失调。这是罕见的病例,其中同时出现僵人综合征和小脑性共济失调的临床症状。在蛋白质印迹分析中,她的血清与大鼠小脑,大脑皮层和脊髓中的65 kDa蛋白反应。 GAD自身抗体可能会导致脊髓以及小脑中的γ-氨基丁酸(GABA)神经元功能受损。

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