Fryns J P, Kleczkowska A, van den Berghe H
Centre for Human Genetics, University of Leuven, Belgium.
Clin Genet. 1988 Jan;33(1):60-2. doi: 10.1111/j.1399-0004.1988.tb04267.x.
In the present report we describe a severely mentally retarded and dysmorphic female child with a de novo 3q/7q reciprocal translocation and loss of band 7q35. This finding supports the hypothesis that the occurrence of mental retardation and/or congenital malformations in de novo autosomal reciprocal translocation may be due to the loss of a small amount of chromatin material during this chromosomal rearrangement.
在本报告中,我们描述了一名患有重度智力发育迟缓及畸形的女童,她存在一条新生的3号染色体与7号染色体相互易位,且7号染色体长臂3区5带缺失。这一发现支持了如下假说:新生常染色体相互易位导致智力发育迟缓及/或先天性畸形的发生,可能是由于在这种染色体重排过程中少量染色质物质的丢失所致。