Literature DB >> 10022457

17Beta-hydroxysteroid dehydrogenase 3 deficiency in women.

B B Mendonca1, I J Arnhold, W Bloise, S Andersson, D W Russell, J D Wilson.   

Abstract

In genetic males, mutation of the 17beta-hydroxysteroid dehydrogenase 3 (17HSD3)gene that is normally expressed in the testes impairs testosterone formation and causes development of male pseudohermaphroditism. We have ascertained seven women who are sisters of men with 17HSD3 deficiency and who are either homozygotes or compound heterozygotes for the same mutations as their affected brothers. Our findings confirm the concept that women with such mutations are asymptomatic.

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Year:  1999        PMID: 10022457     DOI: 10.1210/jcem.84.2.5477

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  8 in total

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Review 4.  Clinical, endocrine, and molecular findings in 17beta-hydroxysteroid dehydrogenase type 3 deficiency.

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  8 in total

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