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马凡氏综合征是一种双侧性晶状体异位合并骨骼肌肉及心血管异常的先天性疾病,与遗传有关。此病已非罕见,国内自1951年至今,在眼科杂志上已有28例报告,其实际发病数当较此更高。我院自1957～1979年22年间共有住院患者19例,今将二者合并共计47例,结合文献作一综合分析,并着重讨论晶状体脱位的治疗,以供防治参考。一、性别 47例中,男性27例,女性20例,男女之比为1.3:1,男略多于女。国外男女之比差不多,如 Rados(1942)统计211例,男性107例,女性104例;Ross(1949)统计118例,男性56例,女性62例。
Marfan syndrome is a congenital bilateral ectopic lens mixed with skeletal muscle and cardiovascular abnormalities, and genetic. This disease is not uncommon. Since 1951, 28 cases have been reported in the ophthalmic period in China. Our hospital from 1957 to 1979, 22 years, a total of 19 cases of hospitalized patients, now the two combined a total of 47 cases, combined with literature for a comprehensive analysis, and focuses on the treatment of lens dislocation for prevention and treatment of reference. First, the gender 47 cases, 27 males and 20 females, male to female ratio of 1.3: 1, slightly more men than women. The ratio of foreign men and women is similar, such as Rados (1942) statistics 211 cases, 107 males and 104 females; Ross (1949) statistics 118 cases, 56 males and 62 females.