Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder:results of a prospective multicenter clinical utility study in the Netherlands

The introduction of rapid exome sequencing (rES) for critically ill neonates admitted to the neonatal intensive care unit has made it possible to impact clinical decision-making. Unbiased prospective studies to quantify the impact of rES over routine genetic testing are, however, scarce. We performed a clinical utility study to compare rES to conventional genetic diagnostic workup for critically ill neonates with suspected genetic disorders. In a multicenter prospective parallel cohort study involving five Dutch NICUs, we performed rES in parallel to routine genetic testing for 60 neonates wit... Mehr ...

Verfasser: Andriessen, Peter
van Zelst-Stams, Wendy A.G.
Vissers, Lisenka E.L.M.
Dokumenttyp: Artikel
Erscheinungsdatum: 2023
Reihe/Periodikum: RADICON-NL consortium , Andriessen , P , van Zelst-Stams , W A G & Vissers , L E L M 2023 , ' Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder : results of a prospective multicenter clinical utility study in the Netherlands ' , European Journal of Pediatrics , vol. 182 , no. 6 , pp. 2683-2692 . https://doi.org/10.1007/s00431-023-04909-1
Schlagwörter: Clinical utility / Diagnostic workflow / Economic evaluation / Neonates / Rapid exome sequencing / Prospective Studies / Exome Sequencing / Humans / Critical Illness / Netherlands / Genetic Testing/methods / Retrospective Studies / Infant / Newborn / Cohort Studies
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29195833
Datenquelle: BASE; Originalkatalog
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Link(s) : https://research.tue.nl/en/publications/39e32709-b690-4e13-a7c1-2264a9946c6e