Clinical trials: Pseudohermaphroditism
Pseudohermaphroditism
Mutation Analysis of 17βhydroxysteroid Dehydrogenase 3 Deficiency
To disclose the molecular pathology of our 3 families with 17βHSD3 deficiency.
- Trial name
- NCT00173654
- Testing
- blood drawing
- Where
- Taiwan
- Volunteers
- 20 people
- Sponsor
- National Taiwan University Hospital
Pseudohermaphroditism, Congenital Adrenal Hyperplasia
Mutation Analysis of 17α-Hydroxylase
To elucidate the molecular pathology of the 4 families with 17α-hydroxylase/17,20-lyase deficiency.
- Conditions
- Pseudohermaphroditism, Congenital Adrenal Hyperplasia, Hypertension
- Trial name
- NCT00172510
- Testing
- blood drawing
- Where
- Taiwan
- Volunteers
- 25 people
- Sponsor
- National Taiwan University Hospital