Genetics and clinical profile of patients with 11-Beta hydroxylase deficiency
Not Applicable
Completed
- Conditions
- Health Condition 1: E250- Congenital adrenogenital disordersassociated with enzyme deficiency
- Registration Number
- CTRI/2019/10/021495
- Lead Sponsor
- A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 13
Inclusion Criteria
Patients with Congenital adrenal hyperplasia due to 11-βhydroxylase deficiency.
Exclusion Criteria
1)Patients with clinical characteristics of 11-β hydroxylase deficiency withoutconfirmed genetic diagnosis.
2)Inadequate Biochemical data.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method clinical and biochemical profile of patients with 11-Beta hydroxylasedeficiencyTimepoint: 1 year
- Secondary Outcome Measures
Name Time Method nilTimepoint: nil