NL-OMON44665招募中不适用
Phenotyping and genotyping of retinal dystrophies in the Netherlands. - Phenotyping of RD.
Oogziekenhuis Rotterdam0 个研究点目标入组 5,100 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 5,100
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
- 2 至 99（—）
入选标准
- •One of the following syndromic or non-syndromic retinal dystrophies:
- •- retinitis pigmentosa,
- •- Leber congenital amaurosis,
- •- cone-rod dystrophy,
- •- cone-dystrophy,
- •- achromatopsia,
- •- Stargardt disease,
- •- choroideremia,
- •- X-linked juvenile retinoschisis,
- •- Usher syndrome,
- •- Bardet Biedl syndrome,
- •- Best disease,
- •- retinal dystrophy closely linked to one of those mentioned above.
- •All modes of inheritance and ages may be considered.
排除标准
- 未提供
研究者
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