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The role of ultrasound in the diagnosis of fetal genetic syndromes. | LitMetric

The role of ultrasound in the diagnosis of fetal genetic syndromes.

Best Pract Res Clin Obstet Gynaecol

Department of Obstetrics and Gynecology, Division of Maternal Fetal Medicine, Washington University in St Louis, St Louis, MO, USA.

Published: April 2014

The use of ultrasound in the prenatal diagnosis of fetal genetic syndromes is rapidly evolving. Advancing technology and new research findings are aiding in the increased accuracy of ultrasound-based diagnosis in combination with other methods of non-invasive and invasive fetal testing. Ultrasound as a screening tool for aneuploidy and other anomalies is increasingly being used throughout pregnancy, beginning in the first trimester. Given the number of recorded syndromes, it is important to identify patterns and establish a strategy for identifying abnormalities on ultrasound. These syndromes encompass a wide range of causes from viral, substance-linked, chromosomal, and other genetic syndromes. Despite the ability of those experienced in ultrasound, it is important to note that not all fetal genetic syndromes can be identified prenatally, and even common syndromes often have no associated ultrasound findings. Here, we review the role of ultrasound in the diagnosis of fetal genetic syndromes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079588PMC
http://dx.doi.org/10.1016/j.bpobgyn.2014.01.005DOI Listing

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