ACTRN12615001113549进行中（未招募）未知
Examination of specific gene mutations and clinical presentation of Oguchi night blindness in four children and their parents in a single Turkish family.
Ankara Ulucanlar Eye Education and Research Hospital0 个研究点目标入组 6 人开始时间: 2015年10月21日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 6
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 12 Years 至 44 Years（—）
- 性别
- All
入选标准
- •The 12-year-old boy (Case 1), 14-year-old girl (Case 2), 16-year-old girl (Case 3), 19-year-old girl (Case 4), 41-year-old woman (Mother) (Case 5), and a 44-year-old man (Father) (Case 6) will be examined.
- •The participants are all members of the same family.
- •A 41-year-old woman (Mother) and a 44-year-old man (Father) had a consanguineous marriage with a 4th degree relative (paternal cousin).
- •Cases 1-4 noticed night blindness initially 3-10 years previously.
- •There were no history of problems with night vision in both father and mother.
排除标准
- •Anyone outside of the selected family is excluded from the study.
研究者
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