Ji X W, Chen X Y, Tan J, Liang H
Department of Medical Genetics, 3rd Army Medical College, Chongqing, Sichuan, China.
Am J Med Genet. 1988 Dec;31(4):783-6. doi: 10.1002/ajmg.1320310409.
Cytogenetic studies on a woman with primary amenorrhea showed an X;15 translocation, karyotype 46,X,t(X;15)(q21;q23). Fifteen percent of the buccal cells showed a normal-sized sex chromatin body. The normal X chromosome was uniformly inactivated. Many balanced X;15 translocations have been reported; however, breakpoints in our patient differ from those reported previously. This case also supports earlier evidence that ovarian development fails when the breakpoint of the X chromosome is in the region X q13-q25 or q13-q27.
对一名原发性闭经女性的细胞遗传学研究显示存在X;15易位,核型为46,X,t(X;15)(q21;q23)。15%的颊黏膜细胞显示有正常大小的性染色质体。正常的X染色体呈均匀失活状态。已有许多平衡型X;15易位的报道;然而,我们这位患者的断点与先前报道的不同。该病例也支持了早期的证据,即当X染色体的断点位于X q13 - q25或q13 - q27区域时,卵巢发育会失败。