A decade of change - lessons learned from prenatal diagnostics in Central Denmark region in 2008-2018.
Dorte Launholt LildballeNaja H BecherElse Marie VestergaardRikke ChristensenStina LouPuk SandagerLars Henning PetersenKasper GadsbøllOlav Bennike Bjørn PetersenIda VogelPublished in: Acta obstetricia et gynecologica Scandinavica (2023)
Chromosomal microarray identified 5.3% trisomies and 3.4% copy number variants, thereby increased the diagnostic yield by more than 64% compared with karyotype only and it also more than halved the turnaround time. Some preliminary concerns proved real, eg prenatal counseling complexity, but these have been resolved over time in a clinical path with expert consultations.