Fetal scans
Early pregnancy scans, NT/FTS, Anomaly/TIFFA, Fetal Echo, Growth, and Advanced 3D/4D scans.
Services Offered
Fetal medicine services for every stage
Explore the scans, procedures, and specialist fetal medicine services offered by Mom & Me. Choose a service and connect with our team for appointment support.
General ultrasound
Specialist scans including Pelvic, TVS, Follicular, Abdomino Pelvic, Abdomen, and Breast scans.
Genetic testing
Genetic counselling, blood markers, NIPT, karyotyping, microarray, and whole exome sequencing.
Fetal procedures
Amniocentesis, CVS, intrauterine blood transfusions (IUBT), reduction, and amniotic patch.
Choose a service to book
Fetal Scan
Early Pregnancy Scan
Conducted between 6-10 weeks of pregnancy to confirm viability, dating, and determine single or multiple pregnancies.
Fetal Scan
NT / FTS Scan
Performed at 11-13 weeks to measure nuchal translucency and screen for chromosomal conditions, combined with blood markers.
Fetal Scan
Anomaly / TIFFA
A detailed scan at 18-22 weeks examining the baby's structural organs, limbs, and fetal anatomy to ensure normal development.
Fetal Scan
Fetal Echo
A specialized ultrasound evaluation at 18-24 weeks focused on the structure, function, and rhythm of the baby's heart.
Fetal Scan
Growth / Doppler
Tracks baby's weight and growth pattern in the third trimester while assessing blood flow and placental efficiency.
Fetal Scan
Advanced 3D & 4D
Advanced 3D surface rendering and real-time 4D motion imaging to visualize fetal facial features and movements.
General USG
Pelvic Scan
Evaluates the uterus, ovaries, and surrounding pelvic structures to check for cysts, fibroids, or source of pain.
General USG
Abdomino Pelvic USG
Comprehensive scan of the abdomen and pelvic cavity, assessing internal organs such as liver, kidneys, and uterus.
General USG
Abdomen USG
Scans the upper abdomen organs including the gallbladder, pancreas, spleen, kidneys, and liver for anomalies.
General USG
TVS (Transvaginal Scan)
Internal pelvic scan offering high-resolution imaging of the cervix, uterus, and ovaries, often used in early pregnancy.
General USG
Follicular Study
Serial scans to track ovarian follicle development, predict ovulation timing, and optimize fertility treatments.
General USG
Cervical Length
Measures cervical length to assess the risk of preterm labor and guide preventative management.
General USG
Breast Ultrasound
Non-invasive screening of breast tissue to evaluate lumps, cysts, or localized pain detected during exam.
Genetic
Genetic Counselling
Professional consultation to assess medical history, explain genetic risks, and guide decision-making for prenatal tests.
Genetic
Double Marker
First-trimester blood test measuring free Beta-hCG and PAPP-A, combined with NT scan to screen for Down syndrome.
Genetic
Quadruple Marker
Second-trimester screening measuring AFP, hCG, uE3, and Inhibin-A to estimate risks of chromosomal and neural tube defects.
Genetic
NIPT / NIPS
Non-invasive prenatal screening analyzing cell-free DNA (cfDNA) in maternal blood for chromosomal abnormalities.
Genetic
Karyotype
A traditional chromosomal test visualizing the full set of chromosomes to detect large structural or numerical changes.
Genetic
Microarray
Chromosomal microarray analysis scanning the genome at high resolution to find microdeletions and microduplications.
Genetic
Whole Exome Sequencing
Advanced genomic test sequencing protein-coding genes to diagnose rare and complex single-gene disorders in the fetus.
Genetic
Sanger Sequencing
Targeted sequencing of specific gene regions, ideal for verifying known familial mutations and genetic variants.
Genetic
Couple Carrier Screening
Pre-pregnancy or early prenatal DNA test to check if partners carry matching mutations for recessive genetic conditions.
Genetic
DNA Storage
Long-term biobanking of purified DNA samples from prenatal procedures for future reference or advanced diagnostic checks.
Procedure
Amniocentesis
A diagnostic procedure analyzing cells from amniotic fluid, performed from 15+ weeks to confirm chromosomal conditions.
Procedure
CVS
Chorionic Villus Sampling takes a tiny placental sample at 11-14 weeks for early diagnostic genetic analysis.
Procedure
Fetal Reduction
A specialized procedure performed in multiple pregnancies to reduce the number of fetuses to improve overall pregnancy outcomes.
Procedure
IUBT
Intrauterine Blood Transfusion, a precise procedure to treat severe fetal anemia by transfusing blood directly into fetal circulation.
Procedure
RFA / Microwave Frequency Ablation
Advanced radiofrequency and microwave ablation procedures used in complicated monochorionic twin pregnancies.
Procedure
Amniotic Patch
An innovative therapeutic procedure to seal ruptured membranes and stop amniotic fluid leakage in pre-viability rupture.