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<正> Purpose: To discuss the clinic features of Rieger syndrome, the reasons of making wrong diagnosis , the way of treatment, and the research progress of its molecular characterization and gene mapping of this syndrome.Methods: Two cases of Rieger syndrome which affected a patient and his daughter were studied. Multiple clinical examinations including photography of anterior segment, go-nioscopy and fundus, Humphrey perimetry, A-scan ultrasonography, multiple tonometry in a day and chromosome examination were performed. Most importantly, ultrasonic biomicro-scope(UBM) was first used to show the abnormalities of anterior segment in this syndrome. Results: Gonioscopic examination revealed many mesoderm tissues remained and some parts of the iris adhered to cornea . In addition to hypoplasia of cornea, iris and chamber angle, UBM showed that there was also hypoplasia of ciliary body. The result of the chomosome examination indicated normal.Conclusions: Rieger syndrome is an autosomal-dominated disorder with m
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篇名 RIEGER SYNDROME
来源期刊 眼科学报 学科 医学
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年,卷(期) 1998,(1) 所属期刊栏目
研究方向 页码范围 52-56
页数 5页 分类号 R770.4
字数 语种 中文
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期刊影响力
眼科学报
季刊
1000-4432
44-1119/R
大16开
广东省广州市先烈南路54号
46-304
1985
chi
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1308
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1
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