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Rieger综合征,是以角膜、虹膜和房角中胚叶发育异常,伴有牙齿、骨骼等发育畸形的一种较为少见的疾病。自从Rieger(1934)首次报告以来,国外已陆续有所报告。国内见到刘崇哲(1981)报告一例。邓慧娟(1982)报告四例。现将我们诊治的两例,系一家两代两例报告如下。一、临床病例报告例一:王××,女、12岁。因双眼自幼畏光,伴左眼胀痛,逐渐视力下降8个月入院。患者为第三胎第三产足月顺产。其父患同样眼病,现已双目失明。一兄,一姐均无该种眼病。其父母非近亲婚姻。
Rieger’s syndrome is based on the cornea, iris and corner of the midbrain developmental abnormalities, accompanied by dental, skeletal and other deformities of a relatively rare disease. Since Rieger (1934) first report, there have been reports from abroad. Domestic see Liu Chongzhe (1981) report a case. Deng Huijuan (1982) report four cases. Now we have two cases of diagnosis and treatment, a family of two cases reported as follows. First, the clinical case report Example 1: Wang × ×, female, 12 years old. Because of his childhood photophobia, with left eye pain, gradually decreased vision 8 months admitted to hospital. The third trimester of patients with third trimester full-term follow-up. His father suffering from the same eye disease, is now blind. A brother, a sister have no such kind of eye disease. Their parents are not close relatives.