Understand the importance of genetic screening during pregnancy
Pregnancy brings many questions, and genetic screening can provide answers about potential genetic disorders in your baby. In the first trimester, you may undergo a combination of a fetal ultrasound and a blood test, which helps assess the risk of certain chromosomal issues with your baby. Another option is Non-Invasive Prenatal Testing (NIPT), which can check for chromosomal abnormalities as early as 9 weeks into your pregnancy.
Why Consider Genetic Screening?
If you or your partner have a family history of genetic disorders, it’s strongly recommended to consider genetic testing. You might also want to explore this option if you have previously had a baby with a genetic condition.
Some Genetic Disorders That Can Be Detected Before Birth:-
- Cystic Fibrosis
- Hemophilia A
- Duchenne Muscular Dystrophy
- Polycystic Kidney Disease
- Sickle Cell Disease
- Thalassemia
Screening Methods Available During Pregnancy:
- Alpha-fetoprotein (AFP) test or multiple marker test
- Amniocentesis
- Chorionic Villus Sampling (CVS)
- Non-Invasive Prenatal Testing (NIPT)
Understanding these options can help you and your partner make informed decisions about your pregnancy. If you have any questions or need more information, feel free to reach us out!
