
In a prospective evaluation, Rapid genome sequencing (rGS) was used to improve the care of 48 infants with complex congenital heart disease (CHD) in a cardiac neonatal intensive care unit. The results showed that rGS diagnosed genetic disorders in 27% of cases and led to changes in management in 62% of cases with diagnostic results. This study emphasizes the importance of rGS in CHD and calls for further research on its implementation for a broader population of infants with CHD.
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