Femmenest is a fetal medicine centre in East Delhi/NCR built for one job: tracking your baby's growth and ruling out problems early, so you and your obstetrician always know exactly where things stand. Our fetal medicine program runs from the first trimester right through delivery — NT scans, anomaly scans, fetal echocardiography, growth monitoring, genetic counselling, and invasive testing when it's genuinely needed — under Dr. Sowjanya Aggarwal, who trained directly with the Fetal Medicine Foundation, UK. If you're carrying a high-risk pregnancy, expecting twins, or simply want a clear week-by-week picture of your baby's development, this is the team for it.
Fetal medicine is the branch of obstetrics that focuses specifically on the baby's wellbeing inside the womb — not just the mother's. A fetal medicine specialist reads your scans for structural and genetic clues a routine ultrasound can miss, and steps in with a management plan if something needs closer attention.
You don't need to be told your pregnancy is "high-risk" to benefit from it. Most women who walk through our doors are having a completely ordinary pregnancy and are simply doing the standard screening every obstetrician recommends — the NT scan at 12 weeks, the anomaly scan at 20 weeks. Fetal medicine becomes more central to your care if you fall into any of these groups:
If any of these sound like you, our high-risk pregnancy team works hand-in-hand with the fetal medicine unit, so your obstetric care and your baby's scans are managed by the same coordinated team rather than being scattered across different clinics.
Here's the screening timeline most pregnancies follow, and what each scan is actually checking for:
| Scan / Test | When It's Done | What It Checks |
| Early viability scan | 6–9 weeks | Location of pregnancy, heartbeat, number of babies, dating |
| NT (Nuchal Translucency) scan | 11 weeks to 13 weeks 6 days | Risk markers for Down syndrome and other chromosomal conditions |
| Anomaly scan (Level 2 / TIFFA) | 18–22 weeks | Detailed structural check of brain, heart, spine, kidneys, limbs |
| Fetal echocardiography | Usually 20–24 weeks, or earlier if advised | Detailed assessment of the baby's heart structure and rhythm |
| Growth & Doppler scan | After 28 weeks, repeated as needed | Baby's growth curve, placenta function, blood flow, amniotic fluid |
| Genetic counselling | Any stage, often pre-conception or post-screening | Personal/family risk assessment, explaining test results |
The NT scan measures fluid at the back of your baby's neck. On its own it's a screening tool, not a diagnosis — which is why we usually combine it with a double marker blood test for a more reliable combined risk score. A higher-than-expected NT measurement doesn't mean something is wrong; it means we look closer, usually with NIPT or, if indicated, a diagnostic test.
This is the most detailed scan of the pregnancy and the one most parents have heard of. Over 30–40 minutes, our sonographer and fetal medicine specialist map the baby's brain, spine, heart, kidneys, abdomen, and limbs, along with placental position and amniotic fluid. It's also when most parents get a long, clear look at their baby for the first time — and where most structural concerns, when they exist, are first picked up.
A standard anomaly scan checks the heart, but a fetal echo goes several steps further into the heart's chambers, valves, and blood flow. We recommend it specifically if you have diabetes, a family history of congenital heart disease, conceived via IVF, or if the anomaly scan flagged anything worth a closer look.
If a screening test comes back high-risk, the next step isn't panic — it's a conversation. Our genetic counselling sessions walk you through what your specific result actually means, what NIPT (a blood-based screening test) versus amniocentesis or CVS (diagnostic, slightly invasive) would tell you, and what your real options are at each step. For couples with a known inherited condition or planning IVF, we also discuss PGT/PGD embryo screening as an earlier alternative. Nobody is pushed toward an invasive test unless it's medically warranted — and that's a judgment call your specialist explains in plain language, not jargon.
Femmenest's fetal medicine program is led by Dr. Sowjanya Aggarwal, one of the few fetal medicine specialists in Delhi NCR with a formal clinical fellowship from the Fetal Medicine Foundation (FMF), UK — completed at the Apollo Centre for Fetal Medicine, Delhi. Beyond Femmenest, she has served as a fetal medicine consultant at Maharaja Agrasen Hospital and as a visiting fetal medicine consultant at Motherland Hospital (Noida), Apollo Centre for Fetal Medicine, and Kailash Hospital. She is a life member of the Society of Fetal Medicine, a member of the AOGD's Genetic and Fetal Medicine Sub-Committee, and a member of ISUOG (International Society of Ultrasound in Obstetrics and Gynecology) — credentials that exist specifically to keep a fetal medicine doctor's scanning and risk-assessment skills current.
What this means for you in practical terms:
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📞 Talk to Our Fetal Medicine Team Book your consultation or call [Insert clinic phone number]. We'll confirm your gestational week and tell you exactly which scan to book first.
Most fetal medicine visits are scheduled, routine screening — but contact us promptly, outside your regular schedule, if you notice:
Whether you're due for your first NT scan or you've been told to see a fetal medicine specialist after an earlier result, the next step is the same: book a consultation or call [Insert clinic phone number]. We'll confirm your dates and walk you through exactly what to expect.
Disclaimer: This content is for general informational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Cost figures are indicative and based on prevailing market rates across the NCR region as of 2026; actual costs vary by individual diagnosis, treatment plan, and clinic. Please consult our fertility specialists for guidance specific to your situation.
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