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Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies.

Nathalie BrisonKris Van Den BogaertLuc DehaspeJessica M E van den OeverKatrien JanssensBettina BlaumeiserHilde PeetersHilde Van EschGriet Van BuggenhoutAnnick VogelsThomy de RavelEric LegiusKoen DevriendtJoris R Vermeesch
Published in: Genetics in medicine : official journal of the American College of Medical Genetics (2016)
Shotgun sequencing of cfDNA not only enables the detection of fetal aneuploidies but also reveals the presence of maternal CNVs. Some of those variants are clinically actionable or could potentially be harmful for the fetus. Interrogating the maternal CNV landscape can improve overall pregnancy management, and we propose reporting those variants if clinically relevant. The identification and reporting of such CNVs pose novel counseling dilemmas that warrant further discussions and development of societal guidelines.Genet Med 19 3, 306-313.
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