视神经炎
医学
髓鞘少突胶质细胞糖蛋白
视神经
眼科
视神经脊髓炎
多发性硬化
皮肤病科
儿科
免疫学
实验性自身免疫性脑脊髓炎
标识
DOI:10.1016/s1474-4422(22)00334-9
摘要
In 1991, the Optic Neuritis Study Group defined the typical profile of acute optic neuritis as unilateral visual loss, an afferent pupillary defect, and eye pain, with normal ophthalmoscopy in most cases.1 However, despite advances in imaging and antibody testing, the misdiagnosis of optic neuritis remains a major concern.2
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