17-Ketosteroid Reductase Deficiency

Common Name(s)

17-Ketosteroid Reductase Deficiency, Testosterone 17-beta-dehydrogenase deficiency

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "17-Ketosteroid Reductase Deficiency" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "17-Ketosteroid Reductase Deficiency" returned 1 free, full-text research articles on human participants. First 3 results:

Male hypogonadism with gynecomastia caused by late-onset deficiency of testicular 17-ketosteroid reductase.
 

Author(s): M Castro-Magana, M Angulo, J Uy

Journal: N. Engl. J. Med.. 1993 May;328(18):1297-301.

 

17-Ketosteroid reductase deficiency results in male pseudohermaphroditism because conversion of the weak androgen androstenedione to the more potent androgen testosterone is impaired. If a late-onset form exists, hypogonadism and gynecomastia caused by decreased testosterone production ...

Last Updated: 11 May 1993

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Reviews from the PubMed Database

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The terms "17-Ketosteroid Reductase Deficiency" returned 0 free, full-text review articles on human participants.

 
 
 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Mutation Analysis of 17╬▓hydroxysteroid Dehydrogenase 3 Deficiency
 

Status: Recruiting

Condition Summary: Pseudohermaphroditism

 

Last Updated: 20 Dec 2005

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