Application of copy number variation sequencing in patients with intellectual disability/developmental delay and autistic spectrum disorder.
10.3760/cma.j.cn511374-20220816-00551
- Author:
Jie LEI
1
;
Gang ZHAO
;
Yanke HUANG
;
Min LONG
;
Wei LI
;
Xi DENG
;
Zihan XIU
;
Yanwei XIAO
;
Sifan ZENG
;
Jing ZHANG
Author Information
1. Department of Clinical Laboratory, Nanshan Maternity and Child Health Care Hospital, Shenzhen, Guangdong 518067, China. zhangjing_nsfy@outlook.com.
- Publication Type:Journal Article
- MeSH:
Pregnancy;
Child;
Male;
Humans;
Female;
DNA Copy Number Variations;
Intellectual Disability/genetics*;
Autism Spectrum Disorder/genetics*;
Developmental Disabilities/genetics*;
Abnormal Karyotype
- From:
Chinese Journal of Medical Genetics
2023;40(3):308-316
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To assess the value of copy number variation sequencing (CNV-seq) for the diagnosis of children with intellectual disability (ID), developmental delay (DD), and autistic spectrum disorder (ASD).
METHODS:Forty patients with ID/DD/ASD referred to Nanshan Maternity and Child Health Care Hospital from September 2018 to January 2022 were enrolled. G-banded karyotyping analysis was carried out for the patients. Genomic DNA was extracted from peripheral blood samples and subjected to CNV-Seq analysis to detect chromosome copy number variations (CNVs) in such patients. ClinVar, DECIPHER, OMIM and other database were searched for data annotation.
RESULTS:Among the 40 patients (including 30 males and 10 females), 16, 15 and 6 were diagnosed with ID, DD and ASD, respectively. One patient had combined symptoms of ID and DD, whilst the remaining two had combined ID and ASD. Four patients were found with abnormal karyotypes, including 47,XY,+mar, 46,XY,inv(8)(p11.2q21.2), 46,XX,del(5)(p14) and 46,XX[76]/46,X,dup(X)(p21.1q12). Chromosome polymorphism was also found in two other patients. CNV-seq analysis has detected 32 CNVs in 20 patients (50.0%, 20/40). Pathogenic CNVs were found in 10 patients (25.0%), 15 CNVs of uncertain clinical significance were found in 12 patients (30.0%), and 7 likely benign CNVs were found in 4 patients (10.0%).
CONCLUSION:Chromosome CNVs play an important role in the pathogenesis of ID/DD/ASD. CNV-seq can detect chromosomal abnormalities including microdeletions and microduplications, which could provide a powerful tool for revealing the genetic etiology of ID/DD/ASD patients.
