Fetal medicine & prenatal diagnosis
Our dedicated fetal medicine unit operates to the highest international standards, offering parents the earliest and most accurate information about their baby's health.
Advanced ultrasound
First-trimester NT scan
Combined with blood biochemistry to screen for chromosomal abnormalities with over 90% detection rate.
Fetal anatomy survey (20-week scan)
Detailed, systematic review of all fetal organs and structures.
3D / 4D imaging
Surface rendering for a detailed view of facial features and limb structure.
Fetal growth monitoring
Regular biometry to detect intra-uterine growth restriction (IUGR).
Doppler velocimetry
Assessment of placental and fetal blood flow dynamics.
Prenatal genetic testing
NIPT (non-invasive)
Cell-free fetal DNA analysis from a maternal blood sample from 10 weeks.
Amniocentesis
Performed under ultrasound guidance for definitive chromosomal diagnosis.
Chorionic villus sampling (CVS)
Earlier prenatal diagnosis (11–14 weeks) for high-risk couples.
Fetal blood sampling (cordocentesis)
For specific in-utero assessment and treatment of fetal conditions.
Genetic counselling
Pre-test counselling
Understand the meaning, implications and risks of each test before you proceed.
Post-test counselling
Compassionate, expert support for families navigating complex results.
Carrier screening
Identifying whether parents carry genes for serious heritable conditions.
Recurrence risk assessment
For couples with a previous pregnancy or child affected by a genetic condition.