NL-OMON34693已完成不适用
Recognition of congenital heart defects caused by CHD7 gene mutations - CHD and CHD7
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
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
- •Patients already available at the department of Genetics of the UMCG or a cohort of children with CHD of the department of Paediatric Cardiology of the RUNMC who
- •1.have a congenital heart defect that fits the spectrum of congenital heart defects found in patients with a CHD7-mutation.
- •2.have at least one other feature of CHARGE syndrome
- •3.do not have another known cause of their congenital heart defect
排除标准
- •- Patients with an already identified (genetic) cause of their congenital heart defect.
- •- Patients who do not want to be informed about the result of the CHD7 analysis
研究者
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