Universal chromosomal microarray analysis reveals high proportion of copy number variants in low risk pregnancies.

CONCLUSION: Albeit lower than observed in high risk pregnancies, the background risk of identifying an abnormal clinically significant CMA result in pregnancies at a low a priori risk for these findings is substantial, and should be conveyed to all pregnant women. This article is protected by copyright. All rights reserved. PMID: 32202684 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/32202684?dopt=Abstract

Source: The Ultrasound Review of Obstetrics and Gynecology - March 22, 2020 Category: Radiology Authors: Stern S, Hacohen N, Meiner V, Yagel S, Zenvirt S, Shkedi-Rafid S, Macarov M, Valsky D, Porat S, Yanai N, Frumkin A, Daum H Tags: Ultrasound Obstet Gynecol Source Type: research