| Literature DB >> 19890128 |
Caroline Achard1, Carine Courtillot, Olivier Lahuna, Géri Méduri, Jean-Claude Soufir, Philippe Lière, Anne Bachelot, Hassani Benyounes, Michael Schumacher, Frédérique Kuttenn, Philippe Touraine, Micheline Misrahi.
Abstract
Men with mutations in LHB, the gene encoding the beta subunit of luteinizing hormone (LHB), have azoospermia with absent or few fetal Leydig cells. We report a mutation in LHB in a man and his sister. The man presented with absence of virilization, undetectable luteinizing hormone, and a low serum testosterone level. He had complete spermatogenesis with a normal sperm count. The mutant luteinizing hormone had a low level of partial activity in vitro. We concluded that the residual luteinizing hormone activity, resulting in the expression of steroidogenic enzymes in few mature Leydig cells producing small amounts of intratesticular testosterone (20.2 ng per gram), was sufficient for complete and quantitatively normal spermatogenesis. Copyright 2009 Massachusetts Medical Society.Entities:
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Year: 2009 PMID: 19890128 DOI: 10.1056/NEJMoa0805792
Source DB: PubMed Journal: N Engl J Med ISSN: 0028-4793 Impact factor: 91.245