동공근을 침범한 항 GQ1b 항체 양성의 비전형적 밀러피셔증후군 1예

• 영문명: A Case of Anti-GQ1b-Positive Atypical Miller Fisher Syndrome With Pupil Involvement
• 발행기관: 대한안과학회
• 저자명: 안재환 이슬기,Jae Hwan Ahn, MD, Sul Gee Lee, MD, PhD
• 간행물 정보: 『대한안과학회지』Ophthalmological Society,volume50,number4, 645~648쪽, 전체 4쪽
• 주제분류: 의약학 > 기타의약학
• 파일형태: PDF
• 발행일자: 2009.04.30

영문 초록

Purpose: To report a case of atypical Miller Fisher syndrome with pupil involvement. Case summary: An 18-year-old woman visited our clinic with a headache and blurred vision. Ophthalmic examination revealed a corrected visual acuity of 20/20 in both eyes, with both pupils dilated to 7.5 mm. There was a loss of light reflex and near reflex in both eyes. Ocular motor examination revealed bilateral abduction, and supraduction limitation, and mild adduction limitation. Neurological examination demonstrated hyporeflexia without ataxia. Brain CT, brain MRI, nerve conduction test, CSF study, and thyroid function tests were normal. The serologic anti-GQ1b IgG test was positive. Conclusions: We confirmed a case of atypical Miller Fisher syndrome with an anti-GQ1 antibody test that had pupil involvement, areflexia, and acute ophthlamoparesis. J Korean Ophthalmol Soc 2009;50(4):645-648

키워드

Anti GQ1b IgG antibody, Miller-Fisher syndrome, Pupil