Prenatal ultrasonic characteristics and genetic analysis of fetuses with chromosome 22q11 microdeletion syndrome.
10.3760/cma.j.cn511374-20200331-00222
- Author:
Meiying CAI
1
;
Na LIN
;
Linjuan SU
;
Xiaoqing WU
;
Xiaorui XIE
;
Ying LI
;
Hailong HUANG
;
Liangpu XU
Author Information
1. Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, Fujian 350001, China. xiliangpu@fjmu.edu.cn.
- Publication Type:Journal Article
- MeSH:
22q11 Deletion Syndrome/diagnostic imaging*;
Chromosome Deletion;
Chromosomes, Human, Pair 22/genetics*;
Female;
Fetus;
Genetic Testing;
Humans;
Pregnancy;
Prenatal Diagnosis;
Ultrasonics
- From:
Chinese Journal of Medical Genetics
2021;38(9):853-856
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To analyze the prenatal ultrasonic characteristics and genetic features of 14 fetuses with chromosome 22q11 microdeletion syndrome (22q11DS).
METHODS:4989 fetuses were analyzed by using single nucleotide polymorphism array (SNP array) in the Fujian Maternal and Child Health Hospital from November 2016 to November 2019.
RESULTS:SNP array showed that 11 fetuses had classic 3 Mb microdeletion in 22q11 region, one fetus had 2.0 Mb microdeletion, and two fetuses had 1.0 Mb microdeletion. The 1.0 Mb microdeletion in 22q11 region contains SNAP29 and CRKL genes, which may increase the risk of congenital renal malformation and cardiovascular malformation.
CONCLUSION:Prenatal ultrasonic characteristics of fetuses with 22q11 microdeletion syndrome vary, and SNP array is a powerful tool to diagnose such diseases, which can provide accurate genetic diagnosis and enable prenatal diagnosis.
