Cell-Free Fetal Dna Testing Market to Make Great Impact in Near Future by 2026

Cell-free fetal DNA is an extension of prenatal testing in a safe and non-invasive method. Prenatal tests are used to find any irregularities in a fetus. The two predominant prenatal tests are chorionic villus sampling (CVS) and amniocentesis, both are invasive and could possess harm to the developing fetus, in some cases it can cause miscarriage. Cell-free fetal DNA is a new alternative of prenatal tests. Fetal DNA is found in mother’s blood stream, cell-free fetal DNA enters into the blood stream through the placenta, placenta is a flattened organ in the uterus where maternal blood and fetal blood. The fetal DNA can be split into very acute fragments, less than 200 base pairs on an average. Maternal DNA fragments are also present in the blood. Fetal DNA is first noticed after 22-25 days of fertilization and its concentrations increase as the time period of pregnancy increases. Diagnostic tests for pregnancy using fetal DNA is possible in seventh week of pregnancy. Fetal DNA can be rarely distinguished from the maternal DNA through diagnostic practice. Amniocentesis and chorionic villus sampling prenatal test is possible within 14-20 weeks and 10-13 weeks of pregnancy respectively. Cell-free fetal DNA non-invasive test is used to detect aneuploidy syndromes, fetal Down syndrome and signals a major shift in diagnostic practice and prenatal screening.

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Cell-Free Fetal DNA Testing Market: Drivers and Restraints

The primary factor for the growth of global cell-free fetal DNA testing market is growing awareness in the people andrequirement of safe or low risk obstetric procedures for prenatal testing. The technology which is used in cell-free DNA analysis and its application to prenatal screening for aneuploidy is rapidly changing. The growth of cell-free fetal DNA testing market is primarily attributed to accurate and effective results for aneuploidy screening....