Skip to main content
Log in

Reversible male infertility in late onset congenital adrenal hyperplasia

  • Case Report
  • Published:
Journal of Endocrinological Investigation Aims and scope Submit manuscript

Abstract

We have studied a male patient who presented with secondary infertility. His eldest daughter suffers from late onset congenital adrenal hyperplasia. Based on his hormonal profile, adrenal and gonadal stimulation tests, semen analyses and testicular biopsy he was diagnosed as suffering from the same disease as his daughter. Steroid treatment yielded improvement in all the parameters mentioned above. Four months later his wife became pregnant and he fathered a child. Suppression of gonadotropin secretion due to overproduction of adrenal androgens would appear to be the reason for the failure of testicular maturation and spermatogenesis in this patient. We conclude: 1) glucocorticoid treatment is indicated in infertile males suffering from nonclassical 21-hydroxylase deficiency; 2) Late onset congenital adrenal hyperplasia should be suspected in any male infertility of unknown origin.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Prader A., Zachmann M., Illig R. Fertility in adult males with congenital adrenal hyperplasia due to 21-Hydroxylase deficiency. Acta Endocrinol. (Suppl.) 177: 57, 1973.

    Google Scholar 

  2. Urban M.D., Lee P.A., Migeon C.J. Adult height and fertility in men with congenital virilizing adrenal hyperplasia. N. Engl. J. Med. 299: 1392, 1978.

    Article  PubMed  CAS  Google Scholar 

  3. Wischunsen J., Baker H.W.G., Hudson B. Reversible male infertility due to congenital adrenal hyperplasia. Clin. Endocrinol. (Oxf.) 14: 571, 1981.

    Article  Google Scholar 

  4. Levine L.S., Dupont B., Lorenzen F., Pang S., Pollack M., Oberfield S.E., Kohn B., Lerner A., Cacciari E., Mantero F., Casio A., Scaroni C., Chiumello G., Rondanini G.F., Gargantini L., Giovannelli G., Virdis R., Bartollotta E., Migliori L., Pintor C., Tato L., Barboni F., New M.I. Genetic and hormonal characterization of cryptic 21-Hydroxylase deficiency. J. Clin. Endocrinol. Metab. 53: 1193, 1981.

    Article  PubMed  CAS  Google Scholar 

  5. Miller W.L., Levine L.S., Molecular and clinical advances in congenital adrenal hyperplasia. J. Pediatr. 1: 111, 1987.

    Google Scholar 

  6. Drucker S., New M.I. Nonclassic adrenal hyperplasia due to 21-Hydroxylase deficiency. The Pediatr. Clin. North Am. 34: 1067, 1987.

    CAS  Google Scholar 

  7. Bonaccorsi A.C., Adler I., Figueiredo J.G. Male infertility due to congenital adrenal hyperplasia: testicular biopsy findings, hormonal evaluation and therapeutic results in three patients. Fertil. Steril. 47: 664, 1987.

    PubMed  CAS  Google Scholar 

  8. Mirski H.A., Hines J.H. Infertility in man with 21-Hydroxylase deficient congenital adrenal hyperplasia. J. Urol. 142: 111, 1989.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Augarten, A., Weissenberg, R., Pariente, C. et al. Reversible male infertility in late onset congenital adrenal hyperplasia. J Endocrinol Invest 14, 237–240 (1991). https://doi.org/10.1007/BF03346799

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF03346799

Key-words

Navigation