Abeliovich D, Dagan J, Kimchi-Sarfaty C, Zlotogora J
Department of Human Genetics, Hadassah Hebrew University Hospital, Hebrew University Hadassah Medical School, Jerusalem, Israel.
Am J Med Genet. 1995 Jan 30;55(3):359-62. doi: 10.1002/ajmg.1320550322.
We describe a familial paracentric inversion (X)(q21.2 q24) in a family with 2 male and 2 female carriers. The males were mentally retarded and the females were normal with normal ovarian function. It is suggested that a recessive mental retardation (MR) gene was disrupted by one of the inversion breakpoints, although an X-linked MR gene which by chance is linked to the inv(X) could not be ruled out. In the female carriers of the paracentric inversion a random X-inactivation was demonstrated. The normal ovarian function is an exception to the concept of "critical region" at Xq13-q26.
我们描述了一个家族性臂间倒位(X)(q21.2 q24),该家族中有2名男性和2名女性携带者。男性智力发育迟缓,女性正常且卵巢功能正常。提示一个隐性智力发育迟缓(MR)基因被其中一个倒位断点破坏,尽管不能排除一个偶然与inv(X)连锁的X连锁MR基因。在臂间倒位的女性携带者中,证实了随机X染色体失活。正常的卵巢功能是Xq13-q26“关键区域”概念的一个例外。