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获得性婴儿展神经麻痹与抗 GM2 抗体相关。

Acquired infantile abducens palsy associated with anti-GM2 antibodies.

机构信息

Department of Pediatric Neurology, Alberta Children's Hospital, Calgary, Alberta, Canada.

出版信息

Pediatr Neurol. 2011 Jun;44(6):459-62. doi: 10.1016/j.pediatrneurol.2011.01.021.

Abstract

Anti-ganglioside antibodies have been associated with acquired neuropathies, including Guillain-Barré syndrome. We describe a case of acute abducens nerve palsy acquired 2 weeks after symptoms of upper respiratory tract infection and rash in a 6-month-old. Elevated anti-GM2 ganglioside immunoglobulin M antibodies were detected in the serum. The palsy slowly improved over time, although eventually surgical intervention was required. Elevated anti-GM2 immunoglobulin M antibodies have previously been reported in Guillain-Barré syndrome variants involving sensory and cranial neuropathies, but never in isolated unilateral cranial nerve VI mononeuropathy. Anti-ganglioside antibodies may play a role in the pathogenesis of postinfectious isolated abducens palsy in young children.

摘要

抗神经节苷脂抗体与获得性神经病有关,包括格林-巴利综合征。我们描述了一例 6 个月大的婴儿,在上呼吸道感染和皮疹症状出现后 2 周出现急性外展神经麻痹。在血清中检测到升高的抗 GM2 神经节苷脂免疫球蛋白 M 抗体。尽管最终需要手术干预,但麻痹随着时间的推移逐渐改善。以前曾报道过涉及感觉神经和颅神经病变的格林-巴利综合征变异型中存在升高的抗 GM2 免疫球蛋白 M 抗体,但从未在孤立的单侧颅神经 VI 单神经病中报道过。抗神经节苷脂抗体可能在儿童感染后孤立性外展神经麻痹的发病机制中起作用。

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