Caricamento...
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....
Salvato in:
| Autori principali: | , , , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The Korean Society for Reproductive Medicine
2013
|
| Soggetti: | |
| Accesso online: | 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 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|