Our team provides diagnosis, monitoring, and treatment for a wide spectrum of fetal and maternal complications. Conditions we routinely manage include:
Congenital Anomalies
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.
Intrauterine Growth Restriction (IUGR)
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.
Twin-to-Twin Transfusion Syndrome (TTTS)
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.
Fetal Cardiac Abnormalities
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.
Neural Tube Defects
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.
First-Trimester Screening (NT Scan, Dual Marker Test)
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.
Targeted Anomaly Scan (Level 2 Ultrasound)
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.
Fetal Echocardiography
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.
Chorionic Villus Sampling (CVS) & Amniocentesis
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.
Non-Invasive Prenatal Testing (NIPT)
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.
Doppler Ultrasound for Fetal Well-Being
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.
Intrauterine Fetal Blood Transfusion
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.
Fetal Surgery
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.
Genetic Counselling for High-Risk Pregnancies
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.
Rh Incompatibility
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.