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Marchesani综合征是一种少见的先天性遗传性疾病。国内毛文书(1959)、鲍丽玲等(1966)和张福昆(1974)先后报告共4例,1985年李志辉等报告14例,1986年黄建纲等报告一例,笔者偶见一例并作了术后随访观察,经家系调查又发现2例,现将结果报告如下: 先证者(5):韦××,男,24岁,未婚,农民,1979年12月22日入院,住院号1022.患者自14岁开始两眼朦视,尔后逐年加重.近五个月来右眼常发红,两个多月尚伴有头痛眼胀痛,视物不清。既往无外伤和眼部手术史。患者为第五胎,足月顺产.9
Marchesani syndrome is a rare congenital hereditary disease. Domestic Mao instruments (1959), Bao Liling et al (1966) and Zhang Fukun (1974) reported a total of 4 cases in 1985, Li Zhihui and other reports in 14 cases, 1986 Huang Jian Gang and other reports of a case, I occasionally a case and made a follow-up observation, The investigation of the pedigree also found 2 cases, the results are reported as follows: proband (5): Wei × ×, male, 24 years old, unmarried, farmer, admitted on December 22, 1979, hospital 1022 patients from 14 years old At the beginning of the two eyes, they gradually increased, and the right eye often developed redness in the past five months. Headache and eye pain was also seen in more than two months, with blurred vision. No previous history of trauma and eye surgery. Patients for the fifth child, full-term delivery .9