NCT03283852招募中不适用
Identifying New Genetic Causes to the Disorders of Growth, Puberty and Sex Development
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 1,100
- 试验地点
- 1
- 主要终点
- mutation research
研究概览
简要总结
Disorders of growth, puberty and sex development can have genetic causes. The exome analysis could detect new mutations responsible for these disorders and the frequency of these mutations in these disorders, their association with other malformations.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •congenital growth hormone deficiency
- •puberty disorder
- •gonadal dysgenesis or anorchia
- •primary ovarian failure
- •disorder of sex development
- •subjects related to a patient with one of the above criteria
排除标准
- •environmental or auto-immune cause
结局指标
主要结局
mutation research
时间窗: baseline
frequency of genetic mutation
次要结局
未报告次要终点
研究者
研究点 (1)
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