Precise prenatal diagnostics to identify conditions early, enabling timely and life-saving interventions for both mother and baby.
Identification of a genetic disorder in the fetus can lead to life-saving interventions initiated either prenatally or early after birth.
A prenatal test that can diagnose genetic disorders such as Down syndrome and other chromosomal conditions with high accuracy.
Involves removing and testing a small sample of cells from the placenta to detect chromosomal abnormalities and genetic conditions.
A minimally invasive procedure performed to treat excess amniotic fluid (polyhydramnios) using a thin needle under ultrasound guidance.
A procedure to remove excess fluid from the fetal bladder, performed safely under real-time ultrasound guidance.
Removal of fluid from the fetal chest cavity to relieve pressure on developing lungs and other vital organs.
Cutting-edge interventional therapies for complex fetal conditions, delivered by specialists with a multidisciplinary approach.
Used in higher-order multiple pregnancies to reduce the risk of complications and improve outcomes for remaining fetuses.
Regular ultrasound monitoring between 11–14 weeks for early detection of twin-specific risks and growth discordances.
Helps drain accumulated fluid in fetal lung or bladder conditions, restoring normal developmental conditions in utero.
Specialised interventions for complex twin pregnancies including monochorionic cases requiring expert management.
A life-saving procedure to provide blood directly to the fetus via the umbilical cord in cases of severe fetal anaemia.
Used to treat twin-to-twin transfusion syndrome (TTTS) by sealing abnormal placental blood vessel connections.
Thorough and timely ultrasound examinations across every trimester to monitor your baby's health, growth, and development.
A transvaginal scan to measure cervical length, helping assess the risk of preterm birth and guide preventive care.
A detailed fetal heart scan, usually performed at 24 weeks to detect structural cardiac abnormalities early.
Confirms the pregnancy, detects the fetal heartbeat, and determines the correct intrauterine location at the earliest stage.
Evaluates the risk of chromosomal abnormalities including Down syndrome by measuring the fluid at the back of the fetal neck.
A detailed scan that examines all fetal organs and structural development to rule out anomalies and reassure parents.
Monitors fetal growth, amniotic fluid levels, placental function, and overall wellbeing in the third trimester.
