Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype

Pi Lin Sung, Sheng Ping Chang, Kuo Chang Wen, Chia Ming Chang, Ming Jie Yang, Lin Chao Chen, Kuan Chong Chao, Chi Ying F. Huang, Yueh Chun Li, Chyi Chyang Lin*

*此作品的通信作者

研究成果: Article同行評審

17 引文 斯高帕斯(Scopus)

摘要

Small supernumerary marker chromosomes (sSMC) originating from chromosome 10 are rare. Only seven cases have been documented, and among those three cases were diagnosed prenatally. We reported on another prenatal diagnosis of a de novo mosaic sSMC in an apparently normal female fetus whose mother had conceived with assisted reproductive technology (ART) procedures. G-banding analysis of amniotic cells was performed. Spectral karyotyping (SKY) and fluorescence in situ hybridization (FISH) studies with chromosome 10-specific alphoid satellite DNA probe were used to identify the chromosome 10 origin of the sSMC. Further FISH study with telomeric sequence probes showed that the sSMC lacked a hybridization signal, suggesting that the marker could be a ring chromosome. FISH studies using BAC clone probes specific for the regions within 10p11.2, 10q11.1, and 10q11.2 showed that the short arm breakpoint was located between 29.8 and 30.7Mb from the 10p telomere, and that the long arm breakpoint was located less than 43.6Mb from the 10p telomere. The karyotype of the fetus was 47,XX,+mar. ish der(10)(SKY+CEP 10+, CTD-2130I7+, RP11-89J23-)/46,XX. Oligonucleotide microarraybased copy number variations (CNV) analysis was also performed and showed a 6.7Mb duplication from 10p11.2 to 10q11.2 (36.2-42.9Mb) with Affymetrix SNP-array 6.0 genotype: arr cgh. 10p11.2q11.2(CN-519687→CN- 541524) X 3. At the 1-year follow-up, the baby did not have any findings of the trisomy 10p syndrome. This observation provided further credence to the concept that additional chromosome material of proximal 10p11.2 may not contribute to the trisomy 10p syndrome phenotype.

原文English
頁(從 - 到)2768-2774
頁數7
期刊American Journal of Medical Genetics, Part A
149
發行號12
DOIs
出版狀態Published - 12月 2009

指紋

深入研究「Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype」主題。共同形成了獨特的指紋。

引用此