Our team provides diagnosis, monitoring, and treatment for a wide spectrum of fetal and maternal complications. Conditions we routinely manage include:
- Congenital Anomalies
- Intrauterine Growth Restriction (IUGR)
- Twin-to-Twin Transfusion Syndrome (TTTS)
- Fetal Cardiac Abnormalities
- Neural Tube Defects
- First-Trimester Screening (NT Scan, Dual Marker Test)
- Targeted Anomaly Scan (Level 2 Ultrasound)
- Fetal Echocardiography
- Chorionic Villus Sampling (CVS) & Amniocentesis
- Non-Invasive Prenatal Testing (NIPT)
- Doppler Ultrasound for Fetal Well-Being
- Intrauterine Fetal Blood Transfusion
- Fetal Surgery
- Genetic Counselling for High-Risk Pregnancies
- Rh Incompatibility
Our fetal medicine doctors use high-resolution imaging and genetic testing to detect structural or chromosomal anomalies. Early detection enables appropriate counselling, further investigations, and sometimes surgical planning or medical intervention.
One of the most common complications monitored by our high-risk pregnancy specialists, IUGR occurs when the fetus is not growing at the expected rate. Management involves Doppler ultrasound surveillance, maternal monitoring, and well-timed delivery.
TTTS is a serious complication in identical twin pregnancies. Our fetal medicine specialists provide early diagnosis and may offer fetal surgery such as laser ablation or fluid drainage to restore balance between the twins.
Through detailed fetal echocardiography, we detect congenital heart defects early, allowing referral to paediatric cardiologists and surgical planning after birth. This multidisciplinary approach ensures immediate postnatal intervention if required.
Conditions like spina bifida and anencephaly are detected during targeted anomaly scans. Our specialists provide families with accurate, sensitive information and help them explore all options, including possible in-utero fetal surgery.
This early screening combines ultrasound and blood markers to assess the risk of chromosomal conditions like Down syndrome. Our pregnancy specialists offer clear interpretation and guidance for further steps if results indicate increased risk.
Performed between 18 and 22 weeks, this is a comprehensive scan to assess the fetal anatomy. It is a key service provided by our fetal medicine specialists in Noida, allowing early detection of abnormalities that may influence pregnancy management.
This specialised ultrasound evaluates the fetal heart's structure and function, especially important in cases with a family history of cardiac disease, maternal diabetes, or abnormal NT findings.
These invasive diagnostic tests are offered when genetic abnormalities are suspected. Our MFM specialists perform these procedures with utmost precision, ensuring minimal risk while obtaining critical diagnostic information.
NIPT is a safe blood test that screens for chromosomal anomalies without posing any risk to the fetus. It is commonly recommended for high-risk pregnancy treatment and is offered as part of our comprehensive fetal medicine services.
This scan assesses blood flow in the umbilical cord, fetal brain, and heart. It is crucial for monitoring intrauterine growth restriction (IUGR) and other conditions managed by our high-risk pregnancy doctors.
Used to treat fetal anaemia, especially in cases of Rh incompatibility, this procedure is performed by highly skilled fetal medicine doctors under real-time ultrasound guidance.
For select cases such as spina bifida repair or TTTS, our team offers in-utero surgical options, in collaboration with neonatal and surgical specialists. These cutting-edge procedures enhance postnatal outcomes significantly.
We offer professional genetic counselling to parents when screening tests show increased risk or if there's a known family history of genetic disorders. Counselling helps families make informed decisions about further testing or interventions.
Our fetal medicine specialists provide vigilant monitoring and treatment for Rh-negative mothers, including prophylactic immunoglobulin administration and fetal surveillance to prevent haemolytic disease of the newborn.
Apollo Hospitals, Noida is equipped with next‑generation imaging and interventional tools that enable accurate diagnostics and precision treatment — key pillars of world-class fetal medicine care.
- 4D Ultrasound
- High-Resolution Fetal MRI
- Digital Doppler Imaging
- Invasive Procedure Suites
We use cutting-edge 4D ultrasound to visualise fetal anatomy in real-time motion. This helps in the early detection of structural abnormalities, behavioural assessment, and parent bonding, especially in complex cases managed by fetal medicine doctors.
In cases where ultrasound results are inconclusive or further detail is needed especially for central nervous system or thoracic anomalies fetal MRI provides enhanced imaging. Our radiology team works hand-in-hand with fetal medicine doctors for comprehensive diagnosis and surgical planning.
Doppler studies help assess blood flow in key fetal vessels, aiding in the management of conditions like IUGR, preeclampsia, and fetal anaemia. Our MFM specialists use digital Doppler imaging for precise evaluation of fetal well-being throughout pregnancy.
Our specialised suites are designed for safe and sterile performance of invasive procedures such as amniocentesis, CVS, intrauterine transfusions, and fetal shunt placements. These high-risk procedures are performed under continuous ultrasound guidance by expert fetal medicine doctors.
Apollo Hospitals, Noida meets the highest standards in maternal and fetal care.
- Fetal Medicine Foundation (FMF) Certified Our fetal medicine doctors are FMF-accredited, ensuring adherence to global protocols in fetal ultrasound and screening.
- Ultrasound & Genetic Testing Accreditation Our imaging and genetics labs meet international standards for accuracy and safety in prenatal diagnostics.
- NICU & Fetal Unit Certification Our NICU and maternal-fetal care units are certified for advanced critical care, making us a preferred centre for high-risk pregnancy treatmentand preterm delivery support.
Fetal medicine scans are typically recommended at key stages of pregnancy. The nuchal translucency (NT) scan is done between 11–14 weeks, followed by the targeted anomaly scan at 18–22 weeks. Additional scans may be advised based on your history, risk factors, or referral from your pregnancy specialist. If you're carrying twins or have a high-risk pregnancy, more frequent scans may be scheduled by your fetal medicine doctor.
Yes, when performed by trained fetal medicine specialists, amniocentesis is generally safe and carries a very low risk of complications (less than 1%). The procedure is guided by real-time ultrasound and involves withdrawing a small sample of amniotic fluid for genetic analysis. It is often offered to women with abnormal screening results or those needing a definitive diagnosis in high-risk pregnancies.
If a structural or genetic anomaly is detected, our fetal medicine doctors provide detailed counselling and organise further tests if needed. You’ll be supported by a multidisciplinary team including genetic counsellors, obstetricians, neonatologists, and if necessary, paediatric surgeons. We help you understand the prognosis, treatment options, and support services available to make informed decisions with confidence and compassion.
Yes, many twins can be delivered vaginally depending on their position, gestational age, and maternal health. However, certain conditions — especially in monochorionic or monoamniotic twins — may require caesarean delivery for safety. Your fetal medicine specialist will guide you based on continuous monitoring and individualised birth planning.
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