KCT0000369招募中未知
Identification of genetic causes and designed therapy by large sized exome data establishment in Charcot-Marie-Tooth disease
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 220
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 1(Year) 至 90(Year)（—）
- 性别
- All
入选标准
- •1. Neuropathic findings by clinical neurological examination
- •2. Peripheral neurpopathy confirmed by electrophisiological test
- •3. Existence of family history or suspect by genetic disease
排除标准
- •1. Identification of the cause of neuropahty
- •2. Confirmed of symptoms by acquired neuropathy
- •3. No family history or condsideration of the disease with genetic causes
研究者
相似试验
招募中
不适用
Comprehensive genetic analysis to identify causative mutations of diseases in the field of pediatric surgeryJPRN-UMIN000038902agoya University Graduate school of Medicine Department of Pediatric Surgery100
招募中
Unknown
Investigating for causative genes in patients with chronic intestinal pseudo obstructiochronic intestinal pseudo obstructionJPRN-UMIN000052227International university of health and welfare Narita Hospital100
招募中
不适用
Discover of severe disease-related genes and disease-susceptibility genes of cryptococcosisJPRN-UMIN000006068agasaki University Graduate School of Biomedical Sciences100
尚未招募
Unknown
Genetics of margin-negative Oral Squamous Cell Carcinoma surgical resection.CTRI/2023/11/060253ICMR
已完成
不适用
Identification of the genetic pathways involved in patients overreacting to radiotherapyNL-OMON35606MAASTRO clinic6