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Prenatal Diagnosis Centre

Finding the Answer
Before Your Baby Is Born

Comprehensive fetal diagnosis at Mayflower brings together every modality of modern prenatal medicine — high-end ultrasound, fetal echo, neurosonography, Doppler, and invasive testing when needed — under the care of one specialist who has personally evaluated more than 20,000 fetuses.

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Central India's First Fetal Medicine Specialist Dr. Kunda Shahane — FMF (London) certified · FIFM · Founder, IIFM Nagpur
Section 01

What is Fetal Diagnosis?

Fetal diagnosis is the structured, specialist-led evaluation of an unborn baby to detect, characterise and counsel on any condition that may affect development, delivery or postnatal life. It is the foundation on which every other decision in fetal medicine is built.

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More than a scan

A routine antenatal ultrasound checks growth and position. A fetal diagnostic evaluation is a different exercise altogether — systematic, protocol-driven, and performed by a specialist trained specifically to interpret what the images mean for your baby's future.

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Built around your situation

No two pregnancies arrive at our clinic for the same reason. Each diagnostic plan is shaped around the specific concern — a high-risk screening result, an abnormal finding elsewhere, a previous affected baby, a family history, or simply the wish for an expert second opinion.

At a GlanceDetails
What it isSpecialist prenatal diagnostic evaluation by a fetal medicine consultant
Who performs itDr. Kunda Shahane — Central India's first fetal medicine specialist, FMF (London) certified
Conditions coveredStructural, chromosomal, genetic, infective and growth disorders
Modalities used2D/3D/4D ultrasound, Doppler, fetal echo, neurosonography, NIPT, amniocentesis, CVS, cordocentesis
EquipmentGE Voluson Signature Expert — AI-enabled premium fetal ultrasound
Typical duration30–60 minutes for the scan + dedicated counselling time
Report & follow-upDetailed report shared with referring obstetrician; in-person counselling for every significant finding
Section 02

The Five Domains of Fetal Diagnosis

Conditions affecting a baby before birth fall into five broad families. Each requires a different diagnostic approach — and each is addressed under one roof at Mayflower.

01

Structural Anomalies

Conditions where an organ or body part has not formed normally — the largest category, and the one detailed ultrasound is best placed to identify.

  • Congenital heart defects (CHD)
  • Brain & spine anomalies
  • Cleft lip and palate
  • Limb & skeletal anomalies
  • Abdominal wall, kidney, lung defects
02

Chromosomal Conditions

Differences in the number or structure of chromosomes. Screened through markers on ultrasound and blood tests; confirmed through invasive testing when indicated.

  • Down syndrome (Trisomy 21)
  • Edwards (T18) & Patau (T13)
  • Turner syndrome & sex chromosome variations
  • Microdeletions (DiGeorge, others)
  • Translocations & structural rearrangements
03

Genetic Syndromes

Single-gene and inherited conditions — usually investigated when there is a family history, parental carrier status, or specific ultrasound findings that point to a syndrome.

  • Thalassaemia & sickle cell disease
  • Spinal muscular atrophy (SMA)
  • Duchenne muscular dystrophy
  • Cystic fibrosis & metabolic disorders
  • Skeletal dysplasias & ciliopathies
04

Fetal Infections

Maternal infections that may cross the placenta and affect the developing baby. Diagnosed through a combination of maternal serology, ultrasound features and, where needed, amniotic fluid testing.

  • TORCH group — toxoplasmosis, rubella, CMV, HSV
  • Cytomegalovirus (CMV) surveillance
  • Parvovirus B19 & fetal anaemia
  • Zika & emerging infections
  • Maternal varicella & syphilis
05

Fetal Growth & Wellbeing Disorders

Conditions where the baby is not growing or thriving as expected. Detected through serial biometry, Doppler studies, and biophysical assessment.

  • Intrauterine growth restriction (IUGR/FGR)
  • Macrosomia (excessively large baby)
  • Oligohydramnios & polyhydramnios
  • Placental insufficiency
  • Twin-to-twin transfusion syndrome (TTTS)
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Whatever the Domain — One Specialist Manages It

Most centres can identify a problem. The harder work begins after — connecting findings across categories, ordering the right next test, coordinating with paediatric subspecialists, and counselling the family honestly. That is what Dr. Kunda Shahane does, in-house, end to end.

Section 03

The Diagnostic Toolkit

Every modality of modern prenatal diagnosis is available at Mayflower — non-invasive screening, advanced imaging and, where genuinely needed, invasive testing. Tests are recommended only when they will meaningfully change management.

🔍 Non-invasive imaging

🧬 Genetic screening & diagnosis

The Imaging Backbone

Every Scan on the GE Voluson Signature Expert

The clarity of a fetal diagnosis depends on the clarity of the image behind it. Mayflower's flagship machine is the GE Voluson Signature Expert — India's most advanced AI-enabled fetal ultrasound system — used on every scan, every patient.

SonoLyst AI Automatically identifies anatomical planes and standardises measurements — reducing variability and the chance of missed views.
fetalHS Heart Tool AI-guided step-by-step assessment of the fetal heart — every cardiac view systematically checked.
4D & STIC Imaging Real-time 3D/4D and Spatio-Temporal Image Correlation for detailed cardiac and structural reconstruction.
Section 04

From Concern to Clarity — How the Pathway Works

Most families arrive at Mayflower along one of three routes: a positive screening test, an abnormal finding on a previous scan, or a clinical history that warrants specialist evaluation. Whichever the route, the path forward follows the same careful sequence.

1
Review & reason

Your existing reports, scans and obstetrician's referral note are reviewed before you arrive. Dr. Kunda begins the consultation already familiar with your case — so the time together is spent on what matters, not on retelling the history.

2
Targeted diagnostic scan

A detailed, protocol-driven ultrasound is performed — the depth and focus shaped by your specific clinical question. For a structural concern, every organ system is systematically examined. For a high NT, FMF protocol is followed. For a growth concern, a complete Doppler workup is added.

3
Honest counselling — same visit

You are not sent home wondering. Findings — whether reassuring or concerning — are explained at the same visit, in language you understand, with the time you need to ask questions. Where appropriate, your partner or family is included in the discussion.

4
Next test, if needed

Where the diagnosis requires further confirmation — a fetal echo, a neurosonography, an MRI referral, NIPT, or invasive testing — the rationale is explained honestly. No test is recommended unless it will meaningfully change what happens next.

5
Multi-disciplinary planning

When a baby has a condition that needs postnatal specialist care, Dr. Kunda coordinates with paediatric cardiologists, paediatric neurologists, neonatologists, geneticists and your delivering obstetrician — so the right team is ready before the baby arrives.

6
Continuity & follow-up

A complete written report goes to your referring obstetrician. Follow-up scans are planned at appropriate intervals. You retain direct access to the clinic on WhatsApp for any anxiety or question between visits.

Section 05

What Dr. Kunda Personally Evaluates

Beyond the standard checklist, the value of a specialist evaluation lies in the subtle observations — and in connecting findings that, on their own, might look unremarkable.

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Full clinical history Maternal medical conditions, medication exposure, family history, consanguinity, previous pregnancies — every relevant detail factored in.
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Every organ system, systematically Head, brain, face, neck, spine, heart, lungs, abdomen, kidneys, bladder, limbs, hands and feet — each examined on a structured protocol.
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Soft markers & subtle findings Findings that may be normal variants — or may point to a larger picture. Their significance interpreted in the context of your overall risk.
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Placenta, cord & liquor Placental position and morphology, cord insertion and vessels, amniotic fluid volume — all assessed for their impact on fetal wellbeing.
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Doppler & flow studies Uterine, umbilical, middle cerebral and ductus venosus Doppler — selected based on the clinical question, never as routine.
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Risk integration & counselling Imaging findings combined with maternal age, biochemistry, NIPT and history to give you a single, considered assessment — not a list of disconnected numbers.
Section 06

Frequently Asked Questions

How is fetal diagnosis different from a routine pregnancy scan?
A routine antenatal scan, often performed at a general radiology centre, checks baby's growth, heartbeat and position. A fetal diagnostic evaluation is performed by a fetal medicine specialist on premium equipment, using structured FMF-standard protocols. Every organ is systematically examined, precise markers are measured, and findings are interpreted in the context of your full clinical picture. Counselling is part of the visit, not a separate referral.
Who should be referred for a fetal diagnostic evaluation?
Women with a positive screening test (high-risk NT, double marker, NIPT), a suspicious finding on a routine ultrasound, a previous baby with an anomaly or genetic condition, advanced maternal age (35 and above), IVF pregnancy, twins or higher-order pregnancy, exposure to teratogenic medication or infection, recurrent pregnancy loss, or any pregnancy classified as high-risk. Self-referral for an expert second opinion is also welcome.
Can every fetal abnormality be detected before birth?
No, and we will always say so honestly. Modern fetal medicine can detect the majority of significant structural and chromosomal conditions when scans are done at the right time, on the right equipment, by an experienced specialist. However, some anomalies only become apparent late in pregnancy or after birth, and many genetic conditions cannot be screened for without a specific clinical reason to look for them. Realistic counselling about what a scan can — and cannot — detect is part of every visit.
How long does a fetal diagnostic evaluation take?
Plan for 30 to 60 minutes for the scan itself, plus additional time for counselling. Complex cases — twin pregnancies, detailed fetal echo, fetal neurosonography — may take longer. We never rush a scan to fit a schedule. The time taken is the time the baby's anatomy requires.
What happens if Dr. Kunda finds something abnormal?
You are never handed a diagnosis and asked to figure it out alone. Dr. Kunda will personally explain what the finding means, what it does not mean, what further tests may help clarify the picture, what outcomes look like for the specific condition, and what choices you have. Time is given for questions — at the same visit, and on follow-up. Where appropriate, paediatric subspecialists are looped in to plan postnatal care.
Is fetal diagnosis safe for the baby?
Non-invasive imaging — ultrasound, Doppler, fetal echo, neurosonography — has an excellent safety record and is the cornerstone of modern fetal diagnosis. Invasive testing (amniocentesis, CVS, cordocentesis) carries a small procedure-related risk, which is openly discussed and weighed against the diagnostic benefit before any test is offered. Invasive testing is recommended only when the information it provides will meaningfully change management.
Will my fetal sex be disclosed during the scan?
No. Mayflower Fetal Medicine Centre strictly complies with the PCPNDT Act, 1994. Fetal sex determination and disclosure are illegal in India and are not performed at this centre under any circumstances. Every scan we do is for medical diagnosis and fetal wellbeing only.
Can a fetal diagnosis evaluation be done for twin pregnancies?
Yes, and twin pregnancies particularly benefit from specialist evaluation. Mayflower has extensive experience in chorionicity determination, TTTS screening and management, selective fetal growth restriction monitoring, and individual anomaly scans for each baby. Twin pregnancies often need more frequent specialist surveillance — usually every 2 weeks for monochorionic twins.
"The phrase 'something is not right' is one of the most frightening sentences in pregnancy. My job is not just to find the answer — it is to sit with you while you understand it. A diagnosis is never just a report; it is the beginning of a conversation about your baby's future. That conversation deserves time, honesty, and a specialist who knows what comes next."
— Dr. Kunda Shahane, MBBS, MS (Obs & Gynae), FIFM, FMF (London)
Central India's First Fetal Medicine Specialist · Mayflower Clinic, Nagpur

Ready for a Specialist Fetal Evaluation?

Send your reports on WhatsApp for a quick review before your visit, or call the clinic directly. Urgent cases — high-risk screening results, abnormal scan findings — are accommodated on priority.

⚖️ PCPNDT Act Notice

Mayflower Fetal Medicine Centre strictly complies with the Pre-Conception and Pre-Natal Diagnostic Techniques (Prohibition of Sex Selection) Act, 1994. All ultrasound and prenatal diagnostic services at this centre are performed exclusively for lawful medical diagnosis and fetal wellbeing. Sex determination and sex-selective practices are strictly prohibited and punishable by law. Disclosure of fetal sex is not performed at this centre under any circumstances.

Medical Disclaimer: The information on this page is for patient education only and does not constitute medical advice. Prenatal diagnostic techniques have inherent limitations — a normal scan or test result does not guarantee the complete absence of any abnormality. Diagnosis and treatment decisions must be individualised, made after clinical examination and review of all relevant investigations by Dr. Kunda Shahane or your treating obstetrician. This website does not provide emergency medical services — in an emergency, contact your nearest hospital immediately.