Fetal Medicine Center, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China.
Gene. 2014 Jan 10;533(2):565-9. doi: 10.1016/j.gene.2013.09.027. Epub 2013 Oct 1.
We applied CMA to detect chromosomal variations during a prenatal diagnosis and detected a 4.5Mb pure microdeletion at 18p11.3 that was not detected by conventional karyotyping. Fluorescent in situ hybridization (FISH) analysis was performed to confirm the deletion. Accurate breakpoints of the deletion in this patient were used to build correlations between monosomy 18p and the concomitant phenotypes, particularly holoprosencephaly (HPE), which is rarely reported in monosomy 18p11.3.
我们应用 CMA 技术在产前诊断中检测染色体变异,并检测到 18p11.3 处的一段 4.5Mb 的纯微缺失,这在传统核型分析中未被检测到。荧光原位杂交(FISH)分析用于确认缺失。该患者缺失的精确断点用于建立单体 18p 与同时存在的表型(特别是前脑无裂畸形)之间的相关性,而单体 18p11.3 中很少报道前脑无裂畸形。