Whole‐genome sequencing analysis in fetal structural anomalies: novel phenotype–genotype discoveries
Adult
Whole Genome Sequencing
DNA Copy Number Variations
Genotype
Ultrasonography, Prenatal
3. Good health
Congenital Abnormalities
Phenotype
Fetus
Pregnancy
Prenatal Diagnosis
Exome Sequencing
Holoprosencephaly
Humans
Female
Genetic Testing
DOI:
10.1002/uog.27517
Publication Date:
2023-10-16T10:24:18Z
AUTHORS (12)
ABSTRACT
ABSTRACTObjectivesThe identification of structural variants and single‐nucleotide variants is essential in finding molecular etiologies of monogenic genetic disorders. Whole‐genome sequencing (WGS) is becoming more widespread in genetic disease diagnosis. However, data on its clinical utility remain limited in prenatal practice. We aimed to expand our understanding of implementing WGS in the genetic diagnosis of fetal structural anomalies.MethodsWe employed trio WGS with a minimum coverage of 40× on the MGI DNBSEQ‐T7 platform in a cohort of 17 fetuses presenting with aberrations detected by ultrasound, but uninformative findings of standard chromosomal microarray analysis (CMA) and exome sequencing (ES).ResultsCausative genetic variants were identified in two families, with an increased diagnostic yield of 11.8% (2/17). Both were exon‐level copy‐number variants of small size (3.03 kb and 5.16 kb) and beyond the detection thresholds of CMA and ES. Moreover, to the best of our knowledge, we have described the first prenatal instance of the association of FGF8 with holoprosencephaly and facial deformities.ConclusionsOur analysis demonstrates the clinical value of WGS in the diagnosis of the underlying etiology of fetuses with structural abnormalities, when routine genetic tests have failed to provide a diagnosis. Additionally, the novel variants and new fetal manifestations have expanded the mutational and phenotypic spectrums of BBS9 and FGF8. © 2023 International Society of Ultrasound in Obstetrics and Gynecology.
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