| Literature DB >> 10022457 |
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.Entities:
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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