4.3 Article

Testis Development and Fertility Potential in Boys with Klinefelter Syndrome

Journal

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.ecl.2015.07.008

Keywords

Testis development; Reproductive options; Klinefelter syndrome; Testicular function; Spermatogenesis; X-chromosome; Sex chromosome aneuploidy

Funding

  1. NIDDK NIH HHS [T32 DK063687] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS050597] Funding Source: Medline

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Klinefelter syndrome (KS) is the leading genetic cause of primary hypogonadism and infertility in men. The clinical phenotype has expanded beyond the original description of infertility, small testes, and gynecomastia. Animal models, epidemiologic studies, and clinical research of male subjects with KS throughout the lifespan have allowed the better characterization of the variable phenotype of this condition. This review provides an overview on what is known of the epidemiology, clinical features, and pathophysiology of KS, followed by a more focused discussion of testicular development and the clinical management of hypogonadism and fertility in boys and men with KS.

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