A case of unusual presentation with anti-glycine receptor (GlyR) and myelin oligodentrocyte glycoprotein (MOG) antibody

IF 1.9 Q3 CLINICAL NEUROLOGY

Clinical Parkinsonism Related Disorders Pub Date : 2023-01-01 DOI:10.1016/j.prdoa.2023.100195

Stefania Kalampokini, Irina Motkova, Panagiotis Bargiotas, Artemios Artemiadis, Panagiotis Zis, Georgios M. Hadjigeorgiou

引用次数: 1

Abstract

Movement disorders can be a prominent feature in autoimmune encephalitis. Here we present a rare case of a 73-year-old woman, who presented with a complex phenotype with encephalopathy, parkinsonism, cervical dystonia, left-sided hemidystonia and hemifacial spasm of subacute onset and was found to have breast cancer and positive anti-Glycine Receptor (GlyR) and Myelin Oligodentrocyte Glycoprotein (MOG) antibodies.

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抗甘氨酸受体(GlyR)和髓鞘少突核细胞糖蛋白(MOG)抗体的异常表现一例

运动障碍可能是自身免疫性脑炎的一个突出特征。在此，我们报告了一例罕见的73岁女性病例，她表现出复杂的亚急性发作性脑病、帕金森综合征、颈部肌张力障碍、左侧肌张力障碍和面肌痉挛表型，并被发现患有乳腺癌症和抗甘氨酸受体（GlyR）和髓鞘寡齿细胞糖蛋白（MOG）抗体阳性。

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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