Central hypogonadism in Klinefelter syndrome: report of two cases and review of the literature
Author:
Funder
Ministero della Salute
Istituto Auxologico Italiano
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s40618-020-01324-3.pdf
Reference61 articles.
1. Kanakis GA, Nieschlag E (2018) Klinefelter syndrome: more than hypogonadism. Metabolism 86:135–144. https://doi.org/10.1016/j.metabol.2017.09.017
2. Bonomi M, Rochira V, Pasquali D et al (2017) Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism. J Endocrinol Invest 40:1. https://doi.org/10.1007/s40618-016-0541-6
3. Spaziani M, Mileno B, Rossi F et al (2018) Endocrine and metabolic evaluation of classic Klinefelter syndrome and high-grade aneuploidies of sexual chromosomes with male phenotype: are they different clinical conditions? Eur J Endocrinol 178:343–352. https://doi.org/10.1530/EJE-17-0902
4. Gravholt CH, Chang S, Wallentin M et al (2018) Klinefelter syndrome: Integrating genetics, neuropsychology, and endocrinology. Endocr Rev 39:389–423. https://doi.org/10.1210/er.2017-00212
5. Chang S, Skakkebæk A, Trolle C et al (2015) Anthropometry in Klinefelter syndrome–multifactorial influences due to CAG length, testosterone treatment and possibly intrauterine hypogonadism. J Clin Endocrinol Metab 100:E508–E517. https://doi.org/10.1210/jc.2014-2834
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