Guo W J, Callif-Daley F, Zapata M C, Miller M E
Department of Medical Genetics, Children's Medical Center, Dayton, Ohio 45404, USA.
Am J Med Genet. 1995 Sep 11;58(3):230-6. doi: 10.1002/ajmg.1320580307.
We report on the clinical and cytogenetic findings in 7 cases of inverted duplication of region 8p11.2p23. The phenotype of inv dup (8p) compiled from this series and the literature (N = 29) consists of severe mental retardation (100%), minor facial alterations (97%), agenesis of the corpus callosum (80%), hypotonia (66%), orthopedic abnormalities (58%), scoliosis/kyphosis (40%), and congenital heart defect (26%). A telomeric deletion of region 8p23.3-pter was confirmed in 3 of our cases studied using fluorescent in situ hybridization with a telomeric probe for 8p. Thus, these karyotypes are inv dup del(8) (qter-->p23.1::p23.1-->p11.2:). Our findings suggest that most cases of inv dup(8p) probably have a telomeric deletion.
我们报告了7例8p11.2p23区域反向重复的临床和细胞遗传学研究结果。根据本系列研究及文献(N = 29)汇总的inv dup(8p)表型包括严重智力发育迟缓(100%)、轻微面部改变(97%)、胼胝体发育不全(80%)、肌张力减退(66%)、骨科异常(58%)、脊柱侧凸/后凸(40%)以及先天性心脏缺陷(26%)。在我们研究的3例病例中,使用8p端粒探针进行荧光原位杂交证实了8p23.3 - pter区域的端粒缺失。因此,这些核型为inv dup del(8) (qter-->p23.1::p23.1-->p11.2:)。我们的研究结果表明,大多数inv dup(8p)病例可能存在端粒缺失。