Prenatal testing, screening, and diagnosis are important tools to help your doctor determine, before birth, whether your fetus has any genetic disorders or congenital anomalies. Tests can be anything from amniocentesis and chorionic villus sampling (CVS) to a simple blood test.

These tests are especially useful to detect trisomies( genetic disorders in baby) for women who are pregnant in their 1st 15 weeks of pregnancy & also for pregnant women above 35 yrs who are at an increased risk for genetic abnormalities.

For more clarifications,

Meet our expert Obstetrician & Gyneacologist

DR.SUNITHA SIVAKUMAR , MD ( og)

Consultation Timings :

Mon to friday : 10 am to 5pm

Saturday : 10 am to 1pm

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