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遗传性视神经萎缩(Leber氏病),病因不明,目前尚无特殊治疗方法,可给予维生素B_1、B_(12)及烟酸等。我院遇见1个家族2例遗传性视神经萎缩,根据病史、眼底表现及家族遗传调查,诊断本病无疑。现报道如下。病例报告例1,周某,女性,13岁,学生,于1983年3月3日入院,住院号831621。主诉:双眼视力明显下降3个月。于1983年1月起,忽感双眼视力急剧下降,伴眼胀、畏光,未经任何治疗。2天后,症状稍减,2月12日又感右眼不适,视力再次明显下降,曾到某院求治,当时诊断为“双眼屈光不正”。在卫生所肌注肌苷、维生素B_(12)等药物,视力仍不
Hereditary optic atrophy (Leber’s disease), the etiology is unknown, there is no special treatment, can be given vitamin B_1, B_ (12) and niacin. I met a family of 2 cases of hereditary optic nerve atrophy, according to medical history, fundus findings and family genetic investigation, the diagnosis of the disease is no doubt. Report as follows now. Case report 1, Zhou, female, 13 years old, student, was admitted on March 3, 1983, hospital number 831621. Chief complaint: binocular vision decreased significantly 3 months. From January 1983 onwards, suddenly felt a sharp decline in binocular vision, with eye swelling, photophobia, without any treatment. After 2 days, the symptom was slightly reduced. On February 12, the right eye was again feeling discomfort, and the visual acuity decreased again. He went to a hospital for medical treatment and was diagnosed as “binocular refractive error” at that time. In instillation in inosine, vitamin B_ (12) and other drugs, visual acuity still not