摘要
目的分析3例16p11.2微缺失综合征胎儿的临床资料,探讨其产前诊断方法及宫内表型。方法回顾3例产前诊断为16p11.2微缺失(593 kb)胎儿的染色体核型分析、单核苷酸多态性微阵列(SNP微阵列)检测结果,分析这3例胎儿的产前超声特点。结果病例1和病例2胎儿羊水染色体核型为46,XX,病例3胎儿羊水染色体核型为46,XY。病例1的SNP微阵列结果为arr[hg19]16p11.2(29,428,531~30,350,748)X1,即16p11.2存在922 kb的缺失。病例2的SNP微阵列结果为arr[hg19]16p11.2(29,591,326~30,176,508)X1,即16p11.2存在585 kb的缺失。病例3的SNP微阵列结果为arr[hg19]16p11.2(29,428,531~30,176,508)X1,即16p11.2存在748 kb的缺失。3例均有关键区域缺失,包含PRRT2、KCTD13、TBX6、HIRIP3、SEZ6L2等候选致病基因。病例1、2产前超声均提示胎儿半椎体畸形、脊柱侧弯,病例3产前超声提示胎儿颈部半透明膜增厚。结论 16p11.2微缺失综合征在产前可出现各个系统超声异常,但椎体畸形最为常见。中国汉族人群产前超声中如果出现胎儿半椎体畸形、脊柱侧弯,应考虑16p11.2微缺失综合征的可能。SNP微阵列分析可以有效地诊断16p11.2微缺失综合征,明确其断裂点以及所涉及的基因,有助于分析其基因型与表型的对应关系。
Objective To analyze 3 cases of 16p11.2 deletion syndrome diagnosed prenatally,and to define the prenatal phenotypes of this syndrome.Methods The results of G-banded karyotyping and single nucleotide polymorphism array(SNP array)of 3 fetuses with 16p11.2 deletion syndrome were reviewed and the prenatal ultrasound of these 3 fetuses were analyzed.Results All amniocenteses revealed normal karyotype.Whereas SNP array detected a 922 kb deletion at 16p11.2[arr[hg19]16p11.2(29,428,531-30,350,748)X1]in fetus 1,a 585 kb deletion at 16p11.2[arr[hg19]16p11.2(29,591,326-30,176,508)X1]in fetus 2,and a 748 kb deletion at 16p11.2[arr[hg19]16p11.2(29,428,531-30,176,508)X1]in fetus 3.All deletions have overlapped with the critical region of chromosome 16p11.2 deletion syndrome and involved candidate genes such as PRRT2,KCTD13,TBX6,HIRIP3 and SEZ6L2. Prenatal ultrasound of fetus 1 and 2 showed hemirertebra and scoliosis, and prenatal ultrasound offetus 3 showed increased nuchal translucency (NT). Conclusions Chromosome 16p11.2 deletion syndrome couldbe seen in several types of prenatal ultrasound abnormalities, and vertebral anomalies are the most frequent. If theprenatal ultrasound showed hemirertebra and scoliosis in Chinese Han population, chromosome 16p11.2 deletionsyndrome could be put into consideration. SNP array can efficiently detect chromosome 16p11.2 deletion syndromeand accurately map the breakpoints and involved genes, which may facilitate understanding of the genotype andphenotype correlations.
作者
姚妍怡
刘念
李卉
王维鹏
张成成
高唐鑫子
徐淑琴
刘丽君
宋婕萍
Yan-yi Yao;Nian Liu;Hui Li;Wei-peng Wang;Cheng-cheng Zhang;Xin-zi Gaotang;Shu-qin Xu;Li-jun Liu;Jie-ping Song(Medical Genetics Center,Maternal and Child Health Hospital of Hubei Province,Wuhan,Hubei 430070,China)
出处
《中国现代医学杂志》
CAS
2019年第19期33-38,共6页
China Journal of Modern Medicine
基金
湖北省卫生和计划生育委员会联合基金(No:WJ2018H0155)
