A novel causative gene of congenital central hypothyroidism.
Completed
- Conditions
- Central hypothyroidismlow blood levels of thyroid hormone because thyroid gland is insufficiently activated10021112
- Registration Number
- NL-OMON41692
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
- Congenital central hypothyroidism.
- First- or second-degree relative of a patient with congenital central hypothyroidism.
Exclusion Criteria
Carriers of other genetic defects known to cause congenital central hypothyroidism.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method