Fetal Medicine FAQs

The Nuchal Translucency (NT) scan is usually done between 11 to 13 weeks of pregnancy. It helps assess the risk of chromosomal conditions and early structural issues.

Yes. An anatomy scan, typically done around 18 - 22 weeks, checks the baby’s organs, spine, brain, heart, and growth. It is important even in low-risk pregnancies.

Fetal echocardiography is a detailed ultrasound of the baby's heart. It is advised if there is a family history of heart defects, diabetes, infections, or concerns seen in routine scans.

Yes. Ultrasound scans used in fetal medicine are safe and non-invasive when done by trained specialists and within medical guidelines.

Non-invasive tests use the mother’s blood to screen for genetic conditions. Invasive tests like amniocentesis or CVS provide definitive diagnosis but are advised only when medically necessary.

These tests are suggested when screening tests show higher risk, or there is a known genetic condition. The decision is always taken after proper counselling.

A Doppler scan checks blood flow between the mother, placenta, and baby. It helps monitor growth, placental function, and well-being in later pregnancy stages.

In many cases, a referral helps, but you can also consult directly if you are advised advanced scans, genetic screening, or high-risk pregnancy evaluation.

Carry previous reports, prescriptions, and scan records. Follow any instructions given for hydration or timing, and feel free to ask questions during the scan.