Literature DB >> 3082205

Gonadal function in men with the Martin-Bell (fragile-X) syndrome.

G D Berkovitz, D P Wilson, N J Carpenter, T R Brown, C J Migeon.   

Abstract

We evaluated testicular function in 15 men with the Martin-Bell (fragile-X) mental retardation syndrome. Macro-orchidism was present in all subjects. Their mean serum LH and FSH levels and plasma testosterone and dihydrotestosterone levels were normal. The mean plasma levels of androstenedione, 17-hydroxyprogesterone, and progesterone were slightly elevated above the normal range, whereas the plasma levels of dehydroepiandrosterone and dehydroepiandrosterone-sulfate were normal. The response in the levels of plasma testosterone following a 5 day period of hCG stimulation was normal in 8 subjects and there was no abnormal accumulation of androgen precursors. The level of 5 alpha-reductase activity and androgen receptor binding was normal in genital skin fibroblasts derived from 3 of these patients. The response of gonadotropin secretion to GnRH stimulation was normal in the 8 men who were tested. Therefore, our data are consistent with the hypothesis that testicular enlargement in men with the Martin-Bell syndrome is not mediated by hormonal factors.

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Year:  1986        PMID: 3082205     DOI: 10.1002/ajmg.1320230118

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Spermatogenesis in two patients with the fragile X syndrome. I. Histology: light and electron microscopy.

Authors:  R Johannisson; H Rehder; V Wendt; E Schwinger
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

  1 in total

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