Advanced Genetic Screening for a Healthy Pregnancy
Prenatal Genetic Testing helps assess the risk of inherited and chromosomal conditions before your baby is born. At Sattva The Fetal Medicine Centre, we provide comprehensive Prenatal Genetic Testing, advanced fetal ultrasound, genetic counselling, and personalized maternal-fetal care. Our specialists focus on early risk assessment, accurate interpretation of results, and evidence-based pregnancy management to support informed decisions and healthy pregnancy outcomes.
What is Prenatal Genetic Testing?
Prenatal Genetic Testing is a group of screening and diagnostic tests performed during pregnancy to evaluate the likelihood or presence of certain genetic and chromosomal conditions in the developing baby. These tests help identify pregnancies that may require closer monitoring, additional investigations, or specialized care.
Depending on your medical history and pregnancy, testing may include screening tests, advanced ultrasound evaluation, and genetic counselling to provide a comprehensive assessment. Early identification of potential genetic conditions enables timely medical guidance, informed decision-making, personalized pregnancy management, and the best possible care for both mother and baby.
Prenatal genetic testing provides valuable information about your baby's genetic health, helping identify potential risks early and enabling personalized pregnancy care for the best possible outcomes.
At Sattva The Fetal Medicine Centre, we offer comprehensive prenatal genetic testing services, combining advanced screening, detailed fetal imaging, expert genetic counselling, and maternal-fetal medicine expertise. Our goal is to identify potential risks early, provide accurate information, and support personalized pregnancy care for the best possible outcomes.
Personalized counselling to assess genetic risks, explain testing options, and help families make informed pregnancy decisions.
Comprehensive first-trimester screening to evaluate the risk of common chromosomal abnormalities early in pregnancy.
Advanced ultrasound assessment measuring nuchal translucency as part of early prenatal screening.
Specialized ultrasound examination to identify fetal markers associated with genetic and chromosomal conditions.
Comprehensive evaluation of maternal history, family history, screening results, and ultrasound findings to determine pregnancy risk.
Advanced fetal imaging to evaluate your baby's anatomy and detect structural abnormalities during pregnancy.
Ongoing monitoring of fetal growth and specialized care for pregnancies requiring closer surveillance.
Individualized pregnancy counselling with referrals for advanced genetic testing when clinically indicated, ensuring coordinated maternal-fetal care.
