NL-OMON38177已完成不适用
*REGISTRY - an observational study of the European Huntington's Disease Network (EHDN)* - Registry
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 800
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
- •.Individuals with clinical features of HD with a confirmatory family history of HD or with DNA testing results demonstrating the presence of the HD mutation (i.e. a CAG repeat expansion within the HD gene >35 on larger allele)
- •Individuals without clinical features of HD with DNA testing result demonstrating presence of the HD mutation (i.e. CAG repeat expansion within the HD gene >35 on larger allele)
- •First-degree relatives (i.e. parents, siblings, or children) of individuals with HD
- •Second-degree relatives (i.e. grandparents and grandchildren) of participating individuals with HD
- •Family members of participating individuals from category 1 or 2 who are know not to carry the HD mutation (e.g., spouses)
排除标准
- •Subjects who are unable to understand the study protocol or unable to give informed consent, and have no legal representative.
- •Participants with choreic movement disorder other than HD.
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