Application of whole exome sequencing for the diagnosis of early-onset genetic diseases among infants aged 0 ~ 6 months.
10.3760/cma.j.cn511374-20250318-00163
- Author:
Danyan ZHUANG
1
,
2
;
Fei WANG
;
Xiaoli PAN
;
Qi YU
;
Lulu YAN
;
Changshui CHEN
;
Haibo LI
Author Information
1. Central Laboratory for Birth Defect Prevention and Control, the Affiliated Women and Children's Hospital of Ningbo University, Ningbo, Zhejiang 315012, China. lihaibo-775@
2. com.
- Publication Type:Journal Article
- MeSH:
Humans;
Exome Sequencing/methods*;
Infant;
Female;
Male;
Infant, Newborn;
Genetic Diseases, Inborn/diagnosis*;
Genetic Testing/methods*
- From:
Chinese Journal of Medical Genetics
2025;42(5):540-546
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To assess the value of whole exome sequencing (WES) for the diagnosis of early-onset genetic diseases among infants aged 0 to 6 month in Ningbo region.
METHODS:268 infants presented at the Women and Children's Hospital Affiliated to Ningbo University from January 2022 to June 2024 undergoing WES-based genetic testing were enrolled. Peripheral blood samples were collected from the infants and their parents and subjected to WES. Pathogenic variants were identified by clinical manifestations. This study has been approved by the Medical Ethics Committee of the Hospital (Ethics No. EC2023-017).
RESULTS:Among the 268 infants, 124 (46.3%) had phenotype-explaining genetic variants. For 42 family-based WES tests, 20 (47.62%) were abnormal, whilst in 226 single-person WES tests, 104 (46.02%) had abnormalities, with 76 (33.63%) verified by parental testing. In 96 fully family-verified cases, 31 were de novo, 40 were parent-inherited, 25 were single-parent-inherited. These included 35 inborn metabolic errors, 28 rare syndromes, 9 neurodevelopmental disorders, 4 musculoskeletal diseases, 5 congenital deafness, 2 mitochondrial diseases, 4 endocrine diseases, and 9 others. Among these, there were 7 pathogenic copy number variations (all deletions), 3 chromosomal abnormalities, and 85 single-nucleotide variations. One case of Beckwith-Wiedemann syndrome was detected by methylation MLPA. Among the single-nucleotide variants, 114 pathogenic/likely pathogenic variants were identified in 61 genes, with common ones including missense variants (64.04%), frameshifting variants (20.18%) and splicing variants (4.39%).
CONCLUSION:WES can offer effective diagnosis for hereditary diseases with specific/non-specific manifestations. For early-age infants, higher detection rates may be attained for inborn metabolic errors, rare syndromes, neurodevelopmental disorders, congenital deafness, and musculoskeletal diseases. Compared with single-person WES, family-based WES can attain a higher diagnostic efficiency.
