Prenatal Genetic Testing: Safeguarding Your Baby’s Health from the Start
Women’s Care Clinic offers state-of-the-art Prenatal Genetic Testing to help ensure your growing family is healthy and strong. Dr. Manisha Mann Kadyan and her team deploy the most advanced genetic screening available today, delivering early answers about potential genetic disorders so you can move forward with clarity and peace of mind.
The main purpose of prenatal genetic testing is to screen for certain genetic disorders.
Tests that can tell parents whether they carry a gene for certain conditions, such as cystic fibrosis and sickle cell anemia, and might pass it onto their baby.
Carrier tests for conditions such as cystic fibrosis, spinal muscular atrophy, and sickle cell disease can help you understand your risk of having a child with a specific condition.
For a further diagnostic testing, we have amniocentesis and chorionic villus sampling (CVS) that can give us more detailed information regarding the baby chromosome and genetic.
Counseling and Genetic Consultation
The genetics counseling team works with parents in an unbiased way to help them interpret what a positive or negative test result means and will help them work through the decision-making process.
By detecting genetic conditions early on, our testing empowers parents to make healthcare and lifestyle decisions that optimise the health outcomes of both mother and baby.
We hope you will understand the importance of knowing your baby’s genetic health. Our Prenatal Genetic Testing services are provided by experienced professionals who offer accurate, dependable results along with supportive care so that you can feel prepared and relaxed.