Timing : 9AM to 6PM

Appointment : +91 87699 88904

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Welcome To The Fetal Medicine Centre

At Dr. Smita’s Fetal Medicine Centre, we are committed to delivering advanced fetal diagnostic and therapeutic services using the latest 3D, 4D, and exclusive 5D ultrasound technology. Our aim is early detection, accurate diagnosis, and timely intervention to ensure the best possible outcomes for maternal and fetal health.
With a focus on excellence and compassionate care, we specialise in fetal scans, prenatal screening, and invasive procedures, guiding expectant parents to make informed choices for a safe and healthy pregnancy journey.

Early & Accurate Detection

Allows early detection of chromosomal abnormalities, congenital defects, and potential fetal growth issues.

Enhanced Diagnostic Confidence

AI-based analysis reduces human bias, providing accurate and repeatable diagnostic results.

Faster & More Efficient Workflow

Optimises prenatal screening processes, cutting scan duration and enhancing overall patient satisfaction.
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Our Expert Doctor

Meet Dr. Smita Punia

Expert in Fetal Medicine

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MBBS, MS (Obs. & Gyn.) – Gold Medalist

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Fetal Medicine Consultant

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Fellow, V.S. Hospital, Ahmedabad

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Fetal medicine foundation, UK Certified for NT scan

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ICOG-Certified Fellow in Fetal Medicine (India’s First ICOG Certified Fellow) at Paras Advanced Center for Fetal Medicine, Ahmedabad

Dr. Smita Punia is a renowned Obstetrician & Gynaecologist and Fetal Medicine Specialist , skilled in prenatal diagnosis of congenital anomalies and advanced invasive techniques. Her vast experience and dedication make her a respected expert in fetal health and high-risk pregnancies.
Our Services

Our Pregnancy Scans

Pregnancy scans offer vital insights into the baby’s development, identify possible anomalies, and safeguard the health of both mother and baby. Conducted through various techniques at different pregnancy stages, they deliver a complete assessment of fetal growth and overall well-being.


Early Pregnancy Scan (6 to 10 Weeks)

This scan helps confirm the pregnancy and its location, determine gestational age and viability, and assess the number of fetuses along with their early growth and developmental progress.


Nuchal Translucency (NT) Scan (11 to 14 weeks)

This scan evaluates the fluid behind the baby’s neck to assess the risk of chromosomal conditions, including Down syndrome and other genetic abnormalities.

Early Anomaly Scan (16 Weeks)

This scan checks your baby’s organs and structures early in pregnancy, helping doctors detect any major issues for timely treatment and care.

Targeted Imaging for Fetal Anomalies (TIFFA) -Level II Scan (18-24 Weeks)

A detailed ultrasound that evaluates the baby’s anatomy, this scan detects structural abnormalities while monitoring fetal growth and development. Key aspects of this scan include:

  • 1. Assessment of Trisomy 21 risk
  • 2. Evaluation of Pre-eclampsia risk
  • 3. Measurement of cervical length

Third Trimester Growth Scan & Doppler (30 weeks 34 weeks)

This scan monitors fetal growth in the third trimester, checks placental and umbilical cord circulation, measures amniotic fluid, and detects any late-appearing structural anomalies for better assessment of fetal well-being.


Advanced 3D/4D/5D Scan

Using advanced ultrasound imaging, this scan delivers detailed 3D visuals and real-time 4D and 5D videos of the baby, showcasing intricate fetal movements and facial features.

Prenatal Screening Services

NT, NB, DV, Tricuspid Flow & Trisomy Risk Evaluation

Conducted using FMF-certified software, this screening assesses the risk of chromosomal abnormalities such as Down syndrome with high accuracy.

Combined First Trimester Screening

A combination of ultrasound imaging and maternal blood tests performed in the first trimester to evaluate the risk of chromosomal abnormalities.

Quadruple Test

A second-trimester blood test used to estimate the risk of chromosomal abnormalities and neural tube defects in the fetus.

Non-Invasive Prenatal Testing (NIPT)

A maternal blood test that analyses fetal DNA to detect chromosomal abnormalities such as Down syndrome with exceptionally high accuracy.