Therapy of endocrine disease: Testicular function and fertility in men with Klinefelter syndrome: a review

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Therapy of endocrine disease : Testicular function and fertility in men with Klinefelter syndrome: a review. / Aksglaede, L; Juul, A.

I: European Journal of Endocrinology, Bind 168, Nr. 4, 2013, s. R67-76.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Aksglaede, L & Juul, A 2013, 'Therapy of endocrine disease: Testicular function and fertility in men with Klinefelter syndrome: a review', European Journal of Endocrinology, bind 168, nr. 4, s. R67-76. https://doi.org/10.1530/EJE-12-0934

APA

Aksglaede, L., & Juul, A. (2013). Therapy of endocrine disease: Testicular function and fertility in men with Klinefelter syndrome: a review. European Journal of Endocrinology, 168(4), R67-76. https://doi.org/10.1530/EJE-12-0934

Vancouver

Aksglaede L, Juul A. Therapy of endocrine disease: Testicular function and fertility in men with Klinefelter syndrome: a review. European Journal of Endocrinology. 2013;168(4):R67-76. https://doi.org/10.1530/EJE-12-0934

Author

Aksglaede, L ; Juul, A. / Therapy of endocrine disease : Testicular function and fertility in men with Klinefelter syndrome: a review. I: European Journal of Endocrinology. 2013 ; Bind 168, Nr. 4. s. R67-76.

Bibtex

@article{cefb6647ffd248c8adea9d68b9ab1981,
title = "Therapy of endocrine disease: Testicular function and fertility in men with Klinefelter syndrome: a review",
abstract = "Klinefelter syndrome, 47,XXY (KS), is the most frequent sex chromosome aberration in males, affecting 1 in 660 newborn boys. The syndrome is characterized by testicular destruction with extensive fibrosis and hyalinization of the seminiferous tubules resulting in small testes, hypergonadotropic hypogonadism, and azoospermia in the majority of cases. Until recently, infertility was considered an untreatable condition in KS. However, with the development of new advanced assisted reproductive techniques such as testicular sperm extraction (TESE) combined with ICSI it seems that KS patients should no longer be labelled as infertile. Especially, microdissection (micro)-TESE has proved to be an advantageous procedure for the identification of testicular spermatozoa in KS. The aim of this review was to describe current knowledge on the testicular changes occurring in KS, the associated changes in reproductive hormones and spermatogenesis, and the existing possibilities of biological fatherhood in 47,XXY patients.",
author = "L Aksglaede and A Juul",
year = "2013",
doi = "10.1530/EJE-12-0934",
language = "English",
volume = "168",
pages = "R67--76",
journal = "European Journal of Endocrinology",
issn = "0804-4643",
publisher = "BioScientifica Ltd.",
number = "4",

}

RIS

TY - JOUR

T1 - Therapy of endocrine disease

T2 - Testicular function and fertility in men with Klinefelter syndrome: a review

AU - Aksglaede, L

AU - Juul, A

PY - 2013

Y1 - 2013

N2 - Klinefelter syndrome, 47,XXY (KS), is the most frequent sex chromosome aberration in males, affecting 1 in 660 newborn boys. The syndrome is characterized by testicular destruction with extensive fibrosis and hyalinization of the seminiferous tubules resulting in small testes, hypergonadotropic hypogonadism, and azoospermia in the majority of cases. Until recently, infertility was considered an untreatable condition in KS. However, with the development of new advanced assisted reproductive techniques such as testicular sperm extraction (TESE) combined with ICSI it seems that KS patients should no longer be labelled as infertile. Especially, microdissection (micro)-TESE has proved to be an advantageous procedure for the identification of testicular spermatozoa in KS. The aim of this review was to describe current knowledge on the testicular changes occurring in KS, the associated changes in reproductive hormones and spermatogenesis, and the existing possibilities of biological fatherhood in 47,XXY patients.

AB - Klinefelter syndrome, 47,XXY (KS), is the most frequent sex chromosome aberration in males, affecting 1 in 660 newborn boys. The syndrome is characterized by testicular destruction with extensive fibrosis and hyalinization of the seminiferous tubules resulting in small testes, hypergonadotropic hypogonadism, and azoospermia in the majority of cases. Until recently, infertility was considered an untreatable condition in KS. However, with the development of new advanced assisted reproductive techniques such as testicular sperm extraction (TESE) combined with ICSI it seems that KS patients should no longer be labelled as infertile. Especially, microdissection (micro)-TESE has proved to be an advantageous procedure for the identification of testicular spermatozoa in KS. The aim of this review was to describe current knowledge on the testicular changes occurring in KS, the associated changes in reproductive hormones and spermatogenesis, and the existing possibilities of biological fatherhood in 47,XXY patients.

U2 - 10.1530/EJE-12-0934

DO - 10.1530/EJE-12-0934

M3 - Review

C2 - 23504510

VL - 168

SP - R67-76

JO - European Journal of Endocrinology

JF - European Journal of Endocrinology

SN - 0804-4643

IS - 4

ER -

ID: 48483708