CTRI/2019/04/018430
Recruiting
未知
Genotype phenotype correlation in Indian Patientswith Congenital Adrenal Hyperplasia due to 21-α hydroxylase deficiency.
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: E250- Congenital adrenogenital disordersassociated with enzyme deficiency
- Sponsor
- A
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with clinically and biochemically diagnosed Congenital adrenal hyperplasia due to 21\-α Hydroxylase deficiency.
Exclusion Criteria
- •Patientswith congenital adrenal hyperplasiahaving clinical and biochemical diagnosis of 11 Beta Hydroxylase deficiency or 3\-Beta hydroxylase deficiency.
Outcomes
Primary Outcomes
Not specified
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