
Whole Genome Sequencing (WGS) has emerged as a vital tool in prenatal genetic diagnosis, especially in cases of fetal structural anomalies. In a study with 17 families, diagnostic yield reached 11.8% as WGS successfully identified causative genetic variants that standard tests missed. Notably, the study revealed the first prenatal case of FGF8-related holoprosencephaly and facial deformities. These findings demonstrate WGS's clinical value in diagnosing the underlying causes of structural abnormalities in fetuses and contribute to an expanded understanding of genetic disorders.
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