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小角膜病,是一种先天性发育异常。1982年我院门诊曾遇到一病患家族共5例,并对其家族进行了系谱调查。现报告如下。刘春梅女46岁工人患者自幼,两眼视物模糊,此后逐渐加重,尤以近几年更加严重。家族史:母患类似眼病,父健康无眼病,二女一子视力均不良。检查:视力:左右眼均0.08,近视力测不清。眼球小,角膜纵径7mm,横径6mm,透明,瞳孔亦小,虹膜纹理清楚,前房略浅,眼压正常。用1%阿托品散瞳后,
Small keratopathy, is a congenital dysplasia. In 1982 our hospital clinic had encountered a family of patients in 5 cases, and its family pedigree investigation. The report is as follows. Liu Chunmei Female 46-year-old worker patient childhood, both eyes blurred, then gradually increased, especially in recent years more serious. Family history: Maternal similar eye disease, the parent health no eye disease, two women and one child vision are bad. Check: visual acuity: left and right eyes are 0.08, near vision was not clear. The eye is small, corneal longitudinal diameter 7mm, diameter 6mm, transparent, the pupil is also small, clear iris texture, slightly cloudy anterior chamber, intraocular pressure normal. With 1% atropine mydriasis,