Uterine leiomyoma confounding a noninvasive prenatal test result

What's already known about this topic? The noninvasive prenatal testing from maternal blood can be confounded by maternal conditions that lead to structural variants/copy number variations in the genome. What does this study add? This study provides further evidence that the grossly ‘abnormal’...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Prenatal diagnosis 2015-10, Vol.35 (10), p.990-993
Hauptverfasser: Dharajiya, Nilesh G., Namba, Akira, Horiuchi, Isao, Miyai, Shunsuke, Farkas, Daniel H., Almasri, Eyad, Saldivar, Juan-Sebastian, Takagi, Kenjiro, Kamei, Yoshimasa
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:What's already known about this topic? The noninvasive prenatal testing from maternal blood can be confounded by maternal conditions that lead to structural variants/copy number variations in the genome. What does this study add? This study provides further evidence that the grossly ‘abnormal’ and ‘non‐reportable’ noninvasive prenatal testing result due to global genomic changes was attributable to a maternal uterine leiomyoma, in an otherwise normal fetus. The possibility of such adventitious findings is something about which physicians ordering noninvasive prenatal testing for their patients may want to offer pre‐test counseling. © 2015 John Wiley & Sons, Ltd.
ISSN:0197-3851
1097-0223
DOI:10.1002/pd.4629