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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Detalhes bibliográficos
Main Authors: Song, Seung-Hun, Won, Hyung Jae, Yoon, Tae Ki, Cha, Dong Hyun, Shim, Jeong Yun, Shim, Sung Han
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Society for Reproductive Medicine 2013
Assuntos:
Case Report
Acesso em linha: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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