Glial fibrillary acidic protein (GFAP) astrocytopathy, an autoimmune central nervous system disorder characterized by the development of immunoglobulin G reactive with GFAP, has received growing attention in recent years. It is documented that GFAP-immunoglobulin G and other autoantibodies can be both detected in some patients. However, the coexistence of anti-myelin-oligodendrocyte glycoprotein (MOG) and GFAP antibodies is rarely reported.

中文翻译：

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髓鞘少突胶质细胞糖蛋白和神经胶质纤维酸性蛋白免疫球蛋白 G 重叠综合征的轻度表型：模仿患者的病毒性脑膜炎。

胶质纤维酸性蛋白（GFAP）星形细胞病是一种自身免疫性中枢神经系统疾病，其特征是免疫球蛋白 G 与 GFAP 发生反应，近年来受到越来越多的关注。据报道，某些患者体内可同时检测到 GFAP-免疫球蛋白 G 和其他自身抗体。然而，抗髓磷脂少突胶质细胞糖蛋白（MOG）和 GFAP 抗体共存的报道很少。