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Biotechnology has advanced pre-natal diagnostics by enabling early detection of genetic disorders and chromosomal abnormalities in foetuses.
Biotechnology has revolutionised the field of pre-natal diagnostics, providing tools and techniques that allow for the early detection of a wide range of genetic disorders and chromosomal abnormalities. This has been made possible through the development of advanced genetic testing methods, such as amniocentesis, chorionic villus sampling (CVS), and non-invasive prenatal testing (NIPT).
Amniocentesis and CVS are invasive procedures that involve the extraction of amniotic fluid or placental tissue, respectively, for genetic analysis. These procedures can detect chromosomal abnormalities such as Down syndrome, as well as genetic disorders like cystic fibrosis and sickle cell anaemia. However, they carry a small risk of miscarriage.
On the other hand, NIPT is a non-invasive procedure that analyses cell-free foetal DNA (cffDNA) in the mother's blood. This test can detect trisomies (extra chromosomes) and other chromosomal abnormalities with high accuracy, and without the risks associated with invasive procedures. The development of NIPT has been a significant advancement in pre-natal diagnostics, offering a safer and more accurate alternative to traditional methods.
Furthermore, biotechnology has also enabled the development of pre-implantation genetic diagnosis (PGD). This technique is used in conjunction with in-vitro fertilisation (IVF) to screen embryos for genetic disorders before they are implanted in the uterus. PGD allows parents who are carriers of genetic disorders to increase their chances of having a healthy baby.
In addition, advancements in biotechnology have also led to the development of more sophisticated imaging techniques. For instance, 3D and 4D ultrasounds provide detailed images of the foetus, allowing for the detection of physical abnormalities that may indicate genetic disorders.
Overall, the advancements in biotechnology have significantly improved the accuracy and safety of pre-natal diagnostics. These technologies have not only made it possible to detect genetic disorders and chromosomal abnormalities early in pregnancy, but also to do so with minimal risk to the mother and foetus.
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