Prenatal diagnosis and genetic analysis for two Chinese pedigrees carrying large fragment deletions of 13q21.
10.3760/cma.j.cn511374-20220802-00515
- Author:
Min XIE
1
;
Jiangyang XUE
;
Yuxin ZHANG
;
Yingwen LIU
;
Haibo LI
Author Information
1. Central Laboratory of Birth Defects Prevention and Control, Ningbo Women and Children's Hospital, Ningbo, Zhejiang 315012, China. lihaibo-775@163.com.
- Publication Type:Journal Article
- MeSH:
Pregnancy;
Child;
Female;
Humans;
Pedigree;
East Asian People;
Prenatal Diagnosis;
Chromosome Aberrations;
Karyotyping;
Microarray Analysis;
DNA Copy Number Variations
- From:
Chinese Journal of Medical Genetics
2023;40(5):588-592
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the strategies of prenatal diagnosis and genetic counseling for fetuses of two families with large deletions of 13q21.
METHODS:Two singleton fetuses who were diagnosed with chromosome 13 microdeletions by non-invasive prenatal testing (NIPT) at Ningbo Women and Children's Hospital in March 2021 and December 2021 respectively were selected as the study subjects. Chromosomal karyotyping and chromosomal microarray analysis (CMA) were carried on amniotic samples. Peripheral blood samples were collected from the two couples for CMA assay to determine the origin of abnormal chromosomes identified in the fetuses.
RESULTS:The karyotypes of the two fetuses were both normal. CMA revealed that they have respectively harbored heterozygous deletions spanning 11.935 Mb at 13q21.1q21.33 and 10.995 Mb at 13q14.3q21.32, which were respectively inherited from their mother and father. Both deletions had low gene density and lacked haploinsufficient genes, and were predicted to be likely benign variants based on database and literature search. Both couples had opted to continue with the pregnancy.
CONCLUSION:The deletions of the 13q21 region in both families may be of benign variants. As the follow-up time was short, there was no sufficient evidence for the determination of pathogenicity, though our finding may still provide a basis for the prenatal diagnosis and genetic counseling.
