A 47,X,+t(X;X)(p22.3;p22.3)del(X)(p11.23q11.2),Y Klinefelter Variant with Morbid Obesity

Klinefelter syndrome is the most common type of genetic cause of hypogonadism. This syndrome is characterized by the presence of 1 or more extra X chromosomes. Phenotype manifestations of this syndrome are small testes, fibrosis of the seminiferous tubules, inability to produce sperm, gynecomastia,...

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Detalhes bibliográficos
Main Authors: Kim, Youngsook, Kim, Won Jin, Huh, Ji Hye, Lee, Sujin, Kim, Daham, Hong, Jae Won, Lee, Eun Jig
Formato: Artigo
Idioma:Inglês
Publicado em: Yonsei University College of Medicine 2013
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3575972/
https://ncbi.nlm.nih.gov/pubmed/23364994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3349/ymj.2013.54.2.538
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