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• W2991592709 abstract "PurposeTo investigate the impact of rapid-turnaround exome sequencing in critically ill neonates using phenotype-based subject selection criteria.MethodsIntensive care unit babies aged <6 months with hypotonia, seizures, a complex metabolic phenotype, and/or multiple congenital malformations were prospectively enrolled for rapid (<7 day) trio-based exome sequencing. Genomic variants relevant to the presenting phenotype were returned to the medical team.ResultsA genetic diagnosis was attained in 29 of 50 (58%) sequenced cases. Twenty-seven (54%) patients received a molecular diagnosis involving known disease genes; two additional cases (4%) were solved with pathogenic variants found in novel disease genes. In 24 of the solved cases, diagnosis had impact on patient management and/or family members. Management changes included shift to palliative care, medication changes, involvement of additional specialties, and the consideration of new experimental therapies.ConclusionPhenotype-based patient selection is effective at identifying critically ill neonates with a high likelihood of receiving a molecular diagnosis via rapid-turnaround exome sequencing, leading to faster and more accurate diagnoses, reducing unnecessary testing and procedures, and informing medical care." @default.
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• W2991592709 date "2020-04-01" @default.
• W2991592709 modified "2023-10-16" @default.
• W2991592709 title "Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield" @default.
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• W2991592709 doi "https://doi.org/10.1038/s41436-019-0708-6" @default.
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