Caring for Sri Lankan mothers
Guiding healthy pregnancies with trust, expertise, and compassionate support every step.
Fetal Medicine North and East Sri Lanka
Expert Care, Compassionate Guidance
At Fetal Medicine North and East Sri Lanka, we are dedicated to providing expectant mothers and their families with the highest standard of prenatal care. Our clinic brings together advanced technology, specialised expertise, and a deeply compassionate approach to support you at every stage of pregnancy.
From the very first scan to detailed fetal assessments and counselling, our maternal–fetal specialists work closely with you, explaining each step with clarity and kindness. We believe every pregnancy is unique, and our goal is to offer personalised care that gives you confidence, reassurance, and the information you need to make informed decisions for your baby’s health.
Pregnancy Screening & NIPT
We offer Non-Invasive Prenatal Testing (NIPT)—a blood test that screens for common chromosomal conditions (e.g., Down syndrome, Edwards syndrome, Patau syndrome) from as early as 10 weeks with excellent accuracy, all with zero risk to mother or baby.
Diagnostic Procedures
When deeper insight is needed, we offer:
Chorionic Villus Sampling (CVS) — for early chromosomal diagnosis
Amniocentesis — diagnosing genetic or developmental conditions through amniotic fluid sampling
All diagnostic options include pre- and post-test counselling to help you understand the process and implications.
Comprehensive Scan Packages Screening & NIPT
Understanding that care is about more than one scan, we’ve created tailored packages to suit different needs:
Complete Monitoring Package
Ideal for thorough prenatal tracking—from early dating to detailed anatomy and well-being checks.
Core Anatomy Package
High-value selection focusing on growth and structural checks during critical windows.
Enhanced Reassurance Package
Ideal for ongoing peace of mind, adding early scans and multiple well-being evaluations.
(Packages must be booked during the first visit. Multiple individual bookings may not be eligible for package pricing.)
Viability Scan
7–10 weeks
This scan confirms your pregnancy, checks that it is developing inside the uterus, and detects the baby’s heartbeat.
We also measure the embryo to estimate your due date and identify whether you are carrying one baby or twins/multiples.
For many parents, this first scan offers peace of mind and the joy of seeing their baby for the very first time.
Nuchal Scan
11 weeks + 3 days to 13 weeks + 6 days
A specialised ultrasound that measures the fluid-filled space at the back of the baby’s neck.
Combined with maternal age and other markers, it helps assess the chance of certain chromosomal conditions such as Down syndrome, Edwards syndrome, and Patau syndrome.
It is completely safe for both mother and baby and forms part of early pregnancy screening.
Anomaly Scan
20 to 24 weeks
A comprehensive, head-to-toe examination of your baby’s development.
We assess the brain, heart, spine, stomach, kidneys, limbs, and facial structure, as well as the placenta, amniotic fluid levels, and blood flow through the umbilical cord.
This is the most detailed routine scan in pregnancy and an important milestone for monitoring fetal health.
Cardiac Scan
various stages, usually 14–24 weeks
A targeted ultrasound focusing on your baby’s heart.
We check the structure, chambers, and rhythm to identify any congenital heart differences early.
Early detection allows better planning for care before and after birth.
Cervical Scan
14 to 24 weeks
Measures the length of the cervix (neck of the womb) to assess the risk of preterm birth.
If the cervix is shorter than expected, we can offer timely advice, extra monitoring, or treatments to help reduce the risk of early labour.
A safe blood test that looks at your baby’s DNA to check the chance of certain chromosomal conditions, including Down syndrome, Edwards syndrome, and Patau syndrome.
With high accuracy and no risk to you or your baby, NIPT offers reassurance early in pregnancy, and our specialists will guide you through every step.
Chorion villus sampling (CVS) involves the examination of chorionic villi (placental tissue). Both the baby and placenta (afterbirth) originate from the same cell and so the chromosomes present in the cells of the placenta are the same as those of the baby.
Amniocentesis involves the examination of cells in the fluid from around the fetus (amniotic fluid).
The cells in the amniotic fluid originate from the baby and so the chromosomes present in these cells are the same as those of the baby.
Enquire today for compassionate, professional fetal medicine support
Because every pregnancy deserves specialised attention and compassion