Prenatal diagnosis and genetic analysis of seven fetuses with 16p12.2 microdeletion or microduplication
10.3760/cma.j.cn113903-20220713-00707
- VernacularTitle:七例16p12.2微缺失或微重复胎儿的产前诊断和遗传学分析
- Author:
Yazhen MAO
1
;
Yuanbo LIN
;
Yuhong LIN
;
Xinru LIU
;
Xiuqiong HUANG
Author Information
1. 福建医科大学附属福州市第一医院检验科，福州 350009
- Keywords:
Chromosome deletion;
Chromosome duplication;
Chromosomes, human, pair 16;
DNA copy number variations;
Polymorphism, single nucleotide;
Prenatal diagnosis
- From:
Chinese Journal of Perinatal Medicine
2023;26(2):109-112
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To investigate the prenatal ultrasonographic features and diagnosis of 16p12.2 copy number variation (CNV).Methods:This retrospective study recruited seven fetuses with 16p12.2 microdeletion/microduplication in the First Affiliated Hospital of Fujian Medical University from January 2017 to December 2021. Data, including the prenatal diagnostic indications, ultrasound findings, karyotypes, genetic testing and mutation tracing results, pregnancy outcomes, and postnatal follow-up data, were summarized with descriptive statistical analysis.Results:Prenatal ultrasound indicated three fetuses with structural abnormalities, including one case each of multiple malformations, interventricular septal defect, and cleft lip and palate. The other four cases were positive for ultrasonic soft markers involving the heart and kidney. The chromosome karyotypes of the seven fetuses were normal. Single nucleotide polymorphism array (SNP array) results showed that four cases had a 381.7-542.4 kb microdeletion containing three genes ( OTOA, METTL9, and IGSF6) in Online Mendelian Inheritance in Man (OMIM) at 16p12.2 (distal region) and three cases had a 484.0-701.7 kb microdeletion/microduplication containing four OMIM genes ( UQCRC2, CDR2, EEF2K, and POLR3E) at 16p12.2 (proximal region). Five (cases 1, 2, 4, 5, and 6) out of the seven fetuses inherited the variants from their phenotypically normal mother/father, and among them, three (cases 2, 4, and 5) were delivered at term and healthy. Two cases (cases 3 and 7) refused to undergo pedigree verification. Case 3, a full-term infant, underwent ventricular septal defect repair three months after birth, and no abnormality was found at 18 months of age. Conclusions:No specific phenotype presents in fetuses with 16p12.2 microdeletion/microduplication in prenatal diagnosis. OTOA gene is the key gene associated with abnormality in the distal region of 16p12.2. Pedigree analysis is conducive to preventing unnecessary termination of pregnancy.
