Short Communication
Factors Affecting the Clinical Use of Non-Invasive Prenatal Testing
Heather Skirton1* and Leigh Jackson2
1Applied Health Genetics, Faculty of Health and Human Sciences, Plymouth University, UK
2Faculty of Health and Human sciences, Plymouth University, Plymouth, UK
- Corresponding Author:
- Skirton H
Drake Circus, Plymouth, PL4 8AA, UK
E-mail: Heather.skirton@plymouth.ac.uk
Received Date: May 15, 2015 Accepted Date: September 01, 2015 Published Date: September 03, 2015
Citation: Skirton H, Jackson L (2015) Factors Affecting the Clinical Use of Non-Invasive Prenatal Testing. J Clin Diagn Res 3:121. doi:10.4172/2376-0311.1000121
Copyright: © 2015 Skirton H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Non-invasive prenatal testing (NIPT) is a technique first developed in the early 1990’s that enables testing of a fetus for genetic conditions, based on a sample of maternal blood [1]. Small fragments of extracellular DNA from both mother and fetus are present in maternal plasma, and by excluding fragments of maternal origin, the fetus can be tested for sex, aneuploidy and some specific genetic conditions [2]. The main benefits of this type of fetal testing over amniocentesis or chorionic villus sampling are the removal of any risk of miscarriage due to invasive testing and obtaining results in the first trimester [2].