Tan Hüseyin, Caner Ibrahim, Deniz Orhan, Büyükavci Mustafa
University of Atatürk, School of Medicine, Erzurum, Turkey.
Pediatr Neurol. 2003 Oct;29(4):349-50. doi: 10.1016/s0887-8994(03)00281-9.
Miller Fisher syndrome is characterized by a triad of ataxia, ophthalmoplegia, and reduced or absent tendon reflexes, with minimal if any limb weakness. Anti-GQ1b immunoglobulin G antibodies are present in high titers in most patients. Presented is a two-year-old female with Miller Fisher syndrome whose blood serum was negative for anti-GQ1b immunoglobulin G antibodies.
米勒-费希尔综合征的特征为共济失调、眼肌麻痹和腱反射减弱或消失三联征，肢体无力轻微或无。大多数患者抗GQ1b免疫球蛋白G抗体呈高滴度。本文报告一名患米勒-费希尔综合征的两岁女性，其血清抗GQ1b免疫球蛋白G抗体为阴性。
