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,...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Youngsook, Kim, Won Jin, Huh, Ji Hye, Lee, Sujin, Kim, Daham, Hong, Jae Won, Lee, Eun Jig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575972/
https://www.ncbi.nlm.nih.gov/pubmed/23364994
http://dx.doi.org/10.3349/ymj.2013.54.2.538

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575972/
https://www.ncbi.nlm.nih.gov/pubmed/23364994
http://dx.doi.org/10.3349/ymj.2013.54.2.538

Ejemplares similares