CTRI/2019/04/018430招募中未知
Genotype phenotype correlation in Indian Patientswith Congenital Adrenal Hyperplasia due to 21-α hydroxylase deficiency.
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- A
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
- •Patients with clinically and biochemically diagnosed Congenital adrenal hyperplasia due to 21-α Hydroxylase deficiency.
排除标准
- •Patientswith congenital adrenal hyperplasiahaving clinical and biochemical diagnosis of 11 Beta Hydroxylase deficiency or 3-Beta hydroxylase deficiency.
研究者
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