A case of the rare variant of Klinefelter syndrome 47,XY,i(X)(q10)

Klinefelter syndrome is the most common genetic form of male hypogonadism, but the phenotype becomes evident only after puberty. It is characterized by infertility, small testes, sparse body and facial hair, increased body weight, gynecomastia, increased LH and FSH, and a low level of testosterone....

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Bibliografiske detaljer
Main Authors: Song, Seung-Hun, Won, Hyung Jae, Yoon, Tae Ki, Cha, Dong Hyun, Shim, Jeong Yun, Shim, Sung Han
Format: Artigo
Sprog:Inglês
Udgivet: The Korean Society for Reproductive Medicine 2013
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3913897/
https://ncbi.nlm.nih.gov/pubmed/24505564
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5653/cerm.2013.40.4.174
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