NCT00925379已完成不适用
Renal HYPODYSPLASIA;Study of Familial Cases and Search for Predisposing Genes
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 342
- 试验地点
- 1
- 主要终点
- Evaluation of the heritability of renal HYPODYSPLASIA (on the renal ultra sound) and DNA collection to make possible identification of predisposing genes
研究概览
简要总结
Evaluation of the frequency of familial cases of renal HYPODYSPLASIA
详细描述
DNA collection from the propositus and its family. A questionnaire will be filled by the parents to seek other affected individual in the family.With another affected member, DNA collection will be collected from the whole family.
A renal ultrasound will be prescribed for the parents, brothers and sisters.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
入排标准
- 年龄范围
- 3 Months 至 18 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Evaluation of the heritability of renal HYPODYSPLASIA (on the renal ultra sound) and DNA collection to make possible identification of predisposing genes
时间窗: the same day
次要结局
未报告次要终点
研究者
研究点 (1)
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