Testicular dysgenesis syndrome: possible role of endocrine disrupters

Research output: Contribution to journalJournal articleResearch

Standard

Testicular dysgenesis syndrome: possible role of endocrine disrupters. / Bay, Katrine; Asklund, Camilla; Skakkebaek, Niels E; Andersson, Anna-Maria.

In: Best Practice & Research: Clinical Endocrinology & Metabolism, Vol. 20, No. 1, 01.03.2006, p. 77-90.

Research output: Contribution to journalJournal articleResearch

Harvard

Bay, K, Asklund, C, Skakkebaek, NE & Andersson, A-M 2006, 'Testicular dysgenesis syndrome: possible role of endocrine disrupters', Best Practice & Research: Clinical Endocrinology & Metabolism, vol. 20, no. 1, pp. 77-90. https://doi.org/10.1016/j.beem.2005.09.004

APA

Bay, K., Asklund, C., Skakkebaek, N. E., & Andersson, A-M. (2006). Testicular dysgenesis syndrome: possible role of endocrine disrupters. Best Practice & Research: Clinical Endocrinology & Metabolism, 20(1), 77-90. https://doi.org/10.1016/j.beem.2005.09.004

Vancouver

Bay K, Asklund C, Skakkebaek NE, Andersson A-M. Testicular dysgenesis syndrome: possible role of endocrine disrupters. Best Practice & Research: Clinical Endocrinology & Metabolism. 2006 Mar 1;20(1):77-90. https://doi.org/10.1016/j.beem.2005.09.004

Author

Bay, Katrine ; Asklund, Camilla ; Skakkebaek, Niels E ; Andersson, Anna-Maria. / Testicular dysgenesis syndrome: possible role of endocrine disrupters. In: Best Practice & Research: Clinical Endocrinology & Metabolism. 2006 ; Vol. 20, No. 1. pp. 77-90.

Bibtex

@article{e7f902c78d74489d9799860fa4957f28,
title = "Testicular dysgenesis syndrome: possible role of endocrine disrupters",
abstract = "The testicular dysgenesis syndrome (TDS) hypothesis proposes that the four conditions cryptorchidism, hypospadias, impaired spermatogenesis and testis cancer may all be manifestations of disturbed prenatal testicular development. The TDS hypothesis is based on epidemiological, clinical and molecular studies, all suggestive of an interrelation between the different symptoms. The aetiology of TDS is suspected to be related to genetic and/or environmental factors, including endocrine disrupters. Few human studies have found associations/correlations between endocrine disrupters, including phthalates, and the different TDS components. However, for ethical reasons, evidence of a causal relationship between prenatal exposure and TDS is inherently difficult to establish in human studies, rendering the recently developed animal TDS model an important tool for investigating the pathogenesis of TDS. Clinically, the most common manifestation of TDS is probably a reduced sperm concentration, whereas the more severe form may include a high risk of testis cancer. Clinicians should be aware of the interconnection between the different features of TDS, and inclusion of a programme for early detection of testis cancer in the management of infertile men with poor semen quality is recommended.",
author = "Katrine Bay and Camilla Asklund and Skakkebaek, {Niels E} and Anna-Maria Andersson",
year = "2006",
month = mar,
day = "1",
doi = "http://dx.doi.org/10.1016/j.beem.2005.09.004",
language = "English",
volume = "20",
pages = "77--90",
journal = "Best Practice and Research in Clinical Endocrinology and Metabolism",
issn = "1521-690X",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Testicular dysgenesis syndrome: possible role of endocrine disrupters

AU - Bay, Katrine

AU - Asklund, Camilla

AU - Skakkebaek, Niels E

AU - Andersson, Anna-Maria

PY - 2006/3/1

Y1 - 2006/3/1

N2 - The testicular dysgenesis syndrome (TDS) hypothesis proposes that the four conditions cryptorchidism, hypospadias, impaired spermatogenesis and testis cancer may all be manifestations of disturbed prenatal testicular development. The TDS hypothesis is based on epidemiological, clinical and molecular studies, all suggestive of an interrelation between the different symptoms. The aetiology of TDS is suspected to be related to genetic and/or environmental factors, including endocrine disrupters. Few human studies have found associations/correlations between endocrine disrupters, including phthalates, and the different TDS components. However, for ethical reasons, evidence of a causal relationship between prenatal exposure and TDS is inherently difficult to establish in human studies, rendering the recently developed animal TDS model an important tool for investigating the pathogenesis of TDS. Clinically, the most common manifestation of TDS is probably a reduced sperm concentration, whereas the more severe form may include a high risk of testis cancer. Clinicians should be aware of the interconnection between the different features of TDS, and inclusion of a programme for early detection of testis cancer in the management of infertile men with poor semen quality is recommended.

AB - The testicular dysgenesis syndrome (TDS) hypothesis proposes that the four conditions cryptorchidism, hypospadias, impaired spermatogenesis and testis cancer may all be manifestations of disturbed prenatal testicular development. The TDS hypothesis is based on epidemiological, clinical and molecular studies, all suggestive of an interrelation between the different symptoms. The aetiology of TDS is suspected to be related to genetic and/or environmental factors, including endocrine disrupters. Few human studies have found associations/correlations between endocrine disrupters, including phthalates, and the different TDS components. However, for ethical reasons, evidence of a causal relationship between prenatal exposure and TDS is inherently difficult to establish in human studies, rendering the recently developed animal TDS model an important tool for investigating the pathogenesis of TDS. Clinically, the most common manifestation of TDS is probably a reduced sperm concentration, whereas the more severe form may include a high risk of testis cancer. Clinicians should be aware of the interconnection between the different features of TDS, and inclusion of a programme for early detection of testis cancer in the management of infertile men with poor semen quality is recommended.

U2 - http://dx.doi.org/10.1016/j.beem.2005.09.004

DO - http://dx.doi.org/10.1016/j.beem.2005.09.004

M3 - Journal article

VL - 20

SP - 77

EP - 90

JO - Best Practice and Research in Clinical Endocrinology and Metabolism

JF - Best Practice and Research in Clinical Endocrinology and Metabolism

SN - 1521-690X

IS - 1

ER -

ID: 34143651