Cerebellar Ataxia Followed by Stiff Person Syndrome in a Patient with Anti-GAD Antibodies.

Pub Date : 2020-02-08 eCollection Date: 2020-01-01 DOI:10.1155/2020/8454532
Sinali O Seneviratne, Katherine A Buzzard, Belinda Cruse, Mastura Monif
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引用次数: 2

Abstract

Anti-GAD antibody syndrome is a result of the production of antibodies against glutamic acid decarboxylase (GAD), the main enzyme responsible for the production of gamma-aminobutyric acid (GABA). Several neurological manifestations including cerebellar ataxia and stiff person syndrome have been reported in association with anti-GAD antibodies. In this paper, we present a case of a young woman with anti-GAD antibodies who initially presented with cerebellar ataxia followed by stiff person syndrome three and a half years later. Having both cerebellar ataxia and stiff person syndrome is a rare occurrence in anti-GAD antibody syndrome. We emphasise the importance of long-term follow-up of patients with anti-GAD antibody syndrome, as delayed neurological manifestations can occur.

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抗gad抗体患者小脑性共济失调并发僵硬人综合征。
抗谷氨酸脱羧酶(GAD)抗体是产生抗谷氨酸脱羧酶(GAD)抗体的结果,GAD是负责产生γ -氨基丁酸(GABA)的主要酶。一些神经系统的表现,包括小脑性共济失调和僵硬的人综合症,已报道与抗广泛性焦虑症抗体相关。在这篇论文中,我们提出了一个年轻的女性与抗广泛性焦虑症抗体谁最初提出了小脑性共济失调跟着僵硬的人综合征三年半后。同时具有小脑共济失调和僵硬的人综合征是罕见的发生在抗广泛性焦虑症抗体综合征。我们强调长期随访抗广泛性焦虑症患者的重要性,因为延迟的神经系统表现可能发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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