CTRI/2020/05/025128已完成未知
Molecular genetic analysis of Congenital Adrenal Hyperplasia due to 21-hydroxylase deficiency in patients attending tertiary care hospital in Madurai, South India - CAH
MultiDisciplinary Research Units DHR ICMR0 个研究点目标入组 58 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 58
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
入选标准
- •All Congenital Adrenal Hyperplasia patients due to 21 hydroxylase deficiency attending outpatient endocrine clinic of Government Rajaji Hospital, Madurai
排除标准
- •Non 21 hydroxylase deficiency
研究者
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