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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Detalles Bibliográficos
Autores principales: Song, Seung-Hun, Won, Hyung Jae, Yoon, Tae Ki, Cha, Dong Hyun, Shim, Jeong Yun, Shim, Sung Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Reproductive Medicine 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913897/
https://www.ncbi.nlm.nih.gov/pubmed/24505564
http://dx.doi.org/10.5653/cerm.2013.40.4.174

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913897/
https://www.ncbi.nlm.nih.gov/pubmed/24505564
http://dx.doi.org/10.5653/cerm.2013.40.4.174

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