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2 studies found for:    17-beta hydroxysteroid dehydrogenase 3 deficiency
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Rank Status Study
1 Unknown  Mutation Analysis of 17βhydroxysteroid Dehydrogenase 3 Deficiency
Condition: Pseudohermaphroditism
Intervention: Procedure: blood drawing
2 Enrolling by invitation Natural History Study of Patients With Excess Androgen
Conditions: Congenital Adrenal Hyperplasia (CAH);   Familial Male-Limited Precocious Puberty (FMPP)
Intervention:

Study has passed its completion date and status has not been verified in more than two years.