论文部分内容阅读
患者,男,18岁。于1983年2月发现视力锐减就诊。家族史: 父系:祖父、祖母、父亲、叔父、姑母等均正常,兄妹5人有4人患此病。母系:外祖父、母亲、舅、姨、表兄弟,表侄等7人患病。其中两人已摘除晶体。眼部检查:远视力:右0.02;左0.02;近视力:右j3;左j3。双眼角膜清晰,虹膜纹理清,有震颤,前房深,瞳孔4毫米大小,对光反射存在。新福林扩瞳见双眼晶体向鼻下方脱位,6点钟瞳孔缘查见脱位晶体上缘。眼底检查:+160能看清,呈豹纹状,余无明显
Patient, male, 18 years old. In February 1983 found sight sharp reduction treatment. Family history: Paternity: grandfather, grandmother, father, uncle, aunt and so on are normal, brother and sister 5 people have 4 people suffering from the disease. Maternal: grandfather, mother, uncle, aunt, cousin, nephew and other seven people sick. Two of them have removed the crystal. Eye examination: far vision: right 0.02; left 0.02; near vision: right j3; left j3. Eyes clear cornea, iris texture clear, tremor, anterior chamber deep, pupil 4 mm in size, the presence of light reflex. New Fulin dilated eyes to see the lens of the lens dislocation of the nose to the bottom of the nose, 6 o’clock pupil margin check dislocation crystal edge. Fundus examination: +160 can see, was leopard-like, I no obvious