Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3→p23.3 and a rearranged duplication of 8q24.13→qter

被引:25
作者
Fan, YS
Siu, VM
机构
[1] London Hlth Sci Ctr, Dept Lab Med, London, ON N6A 4G5, Canada
[2] London Hlth Sci Ctr, Dept Pediat, London, ON N6A 4G5, Canada
[3] Univ Western Ontario, Dept Pathol, London, ON, Canada
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 102卷 / 03期
关键词
inverted duplication of 8p; duplication of 8q; chromosome; 8; FISH; multiple congenital anomalies; developmental delay;
D O I
10.1002/ajmg.1460
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A derivative chromosome 8 was observed in a newborn boy who presented with low birth weight, multiple congenital anomalies, and dysmorphic face. The der(8) was further characterized at age 18 months by a high resolution G-banding analysis, spectral karyotyping, and fluorescence in situ hybridization (FISH) with multiple DNA probes. The karyotype was described as 46,XY,der (8)(qter-->q24.13::p21.3 --> p23.3::p23.3 --> qter), representing an inverted duplication of region 8p2l.3-->p23.3 and a duplication of region 8q24.13-->qter, which attaches to the duplicated short arm segment at 8p2l.3. Different from previously reported patients with an inverted duplication (8p), no deletion was detected in the distal region of 8p in this case. This young child had manifested a broad nasal bridge, micrognathia, cleft lip, hydrocephalus, partial agenesis of the corpus callosum, Dandy-Walker malformation, congenital heart defects, dysplastic kidneys, hydronephrosis, marked hypotonia, and significant psychomotor retardation. These features are compared with those commonly seen in cases with an inverted duplication of 8p and cases with a partial trisomy of 8q. (c) 2001 Wiley-Liss, Inc.
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页码:266 / 271
页数:6
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