Fetal Medicine (Invasive & Non-Invasive Tests - Amniocentesis and More)

Radiant Diagnostics is a trusted name in maternal-fetal healthcare, offering expert care in Fetal Medicine through a comprehensive range of both invasive and non-invasive prenatal tests. Our fetal medicine unit is equipped with advanced diagnostic technology and is led by highly experienced maternal-fetal medicine specialists.

Our goal is to ensure early detection, accurate diagnosis, and timely intervention for fetal abnormalities, providing expecting parents with the information and support they need to make informed decisions. The invasive procedures we offer include Amniocentesis, Chorionic Villus Sampling (CVS), and Cordocentesis, each carefully performed under ultrasound guidance by trained experts.

For non-invasive assessments, we provide Nuchal Translucency (NT) Scan, First and Second Trimester Screening, Non-Invasive Prenatal Testing (NIPT) for chromosomal disorders like Down syndrome, and detailed fetal anomaly scans. All procedures are explained thoroughly to the expecting parents, ensuring transparency and emotional support throughout the journey.

We go beyond testing and diagnosis to offer a holistic approach by:

Offering genetic counseling for families with a history of genetic disorders.

Providing continuous fetal monitoring in complicated pregnancies.

Working in close collaboration with gynecologists, neonatologists, and pediatric surgeons when required.

Educating parents about prevention strategies for birth defects and fetal infections.

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Frequently asked questions

We offer a complete range of both invasive and non-invasive prenatal tests. Invasive tests include Amniocentesis, Chorionic Villus Sampling (CVS), and Cordocentesis, while non-invasive options include NT Scan, First & Second Trimester Screening, NIPT (Non-Invasive Prenatal Testing), and Fetal Anomaly Scans.

Yes, NIPT is completely safe for both the mother and baby. It is a blood test that analyzes fetal DNA circulating in the mother’s blood to screen for chromosomal conditions such as Down syndrome, without any risk of miscarriage.

Invasive tests are recommended for high-risk pregnancies, such as when abnormal screening results are found, there is a family history of genetic conditions, or the mother is above 35 years of age. These are performed under ultrasound guidance by trained specialists.

Yes, we offer personalized prenatal counseling, genetic counseling, and emotional support. Our team ensures that all procedures are clearly explained and that parents are supported at every step.

We follow a collaborative care approach involving gynecologists, neonatologists, and pediatric surgeons. Continuous fetal monitoring, early diagnosis, and timely interventions are part of our strategy for managing complex pregnancies.
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