Your Baby’s Health Begins with Insightful Screening and Support.
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Explore our range of specialized scans and consultations designed to support you and your baby at every stage of pregnancy. From early reassurance to detailed anomaly scans — every service is delivered with care, clarity, and clinical precision.
Services
First Trimester Scan
The First Trimester Scan is a general early pregnancy evaluation performed in the late first trimester. It confirms key developmental milestones in the fetus. This scan checks the baby's heartbeat, movement, gestational age, and basic anatomy including limbs, head, abdomen, and spine. It also assesses the position of the placenta and the amount of amniotic fluid. If a mother missed earlier scans, this one helps to date the pregnancy and detect any major visible structural issues early on.
​This scan offers an overall look at the baby’s growth and provides the foundation for combining further screening tests.
Nuchal Translucency (NT) Scan
The NT Scan is a specific screening test done during the First Trimester Scan to assess the baby’s risk of chromosomal abnormalities such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13). It measures the nuchal translucency, which is a fluid-filled space at the back of the baby’s neck. A thicker NT measurement can indicate a higher risk of certain genetic conditions.
When combined with maternal blood tests (dual marker), the NT scan provides a risk assessment for genetic abnormalities — this is known as the First Trimester Combined Screening.
This scan doesn't diagnose, but it gives parents a risk score to help decide whether further testing (like NIPT or amniocentesis) is needed.
Anomaly Scan
​It is usually performed between 18 and 22 weeks of pregnancy, the anomaly scan is a detailed examination of the baby’s anatomy. It checks the brain, spine, face, limbs, heart, stomach, kidneys, and other internal organs.
This scan helps detect major structural abnormalities early and ensures that the baby is growing appropriately. It also evaluates the placenta, umbilical cord, amniotic fluid, and cervical length. The anomaly scan is considered one of the most important assessments during pregnancy.
Growth Scan
Growth Scan
​It is conducted in the third trimester, usually after 28 weeks, the growth scan monitors the baby’s development and well-being. It assesses parameters such as the baby’s weight, head circumference, abdominal circumference, and femur length.
The scan also checks the amount of amniotic fluid and the blood flow to the baby using Doppler studies. It’s especially important in high-risk pregnancies or when there’s concern about fetal growth restriction or excess fluid. It guides the doctor in deciding the safest time and mode of delivery.
Fetal Echocardiography
This specialized ultrasound focuses on evaluating the structure and function of the baby’s heart. It is generally recommended between 18 and 24 weeks, especially in cases with risk factors such as maternal diabetes, family history of congenital heart disease, or abnormal findings in routine scans
It provides a detailed view of the heart chambers, valves, and blood flow. Early detection of heart defects can improve planning and care after birth and ensure the baby receives the right treatment at the right time.
Amniocentesis
Amniocentesis is a diagnostic procedure used to detect chromosomal abnormalities, genetic disorders, and certain infections in the baby. During the procedure, a small amount of amniotic fluid — which surrounds and protects the baby — is withdrawn using a thin needle inserted through the mother’s abdomen under continuous ultrasound guidance.
The fluid contains fetal cells and important chemicals that are analyzed in a lab. Amniocentesis is typically recommended when there’s an increased risk from screening tests, advanced maternal age, or a family history of genetic conditions. Though minimally invasive, it’s a safe and highly accurate test when performed by an expert.
​Chorionic Villus Sampling (CVS)
Chorionic Villus Sampling (CVS) is an early diagnostic test used to detect chromosomal abnormalities and certain inherited genetic disorders. In this procedure, a small sample of placental tissue — called chorionic villi — is collected either through the cervix (transcervical) or through the abdomen (transabdominal), both under ultrasound guidance.
Chorionic Villus Sampling (CVS) is an early diagnostic test used to detect chromosomal abnormalities and certain inherited genetic disorders. In this procedure, a small sample of placental tissue — called chorionic villi — is collected either through the cervix (transcervical) or through the abdomen (transabdominal), both under ultrasound guidance.
Understand the Trimester cycle
