Fuse H, Takahara M, Ito H, Shimazaki J
Urol Int. 1986;41(3):235-7. doi: 10.1159/000281207.
A 40-year-old male was referred to the Chiba University Hospital for hypogonadism. He showed many of the phenotypic features of Klinefelter's syndrome. Cytogenetic studies revealed a 48,XXYY karyotype. The significance of the association of this karyotype with incurable skin ulcer is discussed.
一名40岁男性因性腺功能减退被转诊至千叶大学医院。他表现出许多克兰费尔特综合征的表型特征。细胞遗传学研究显示其核型为48,XXYY。本文讨论了这种核型与无法治愈的皮肤溃疡之间关联的意义。