What Is a Genetic Sonogram?

A genetic sonogram is an advanced ultrasound test that evaluates the baby’s risk for chromosomal or genetic conditions. It is usually done between 18 and 22 weeks of pregnancy. The scan helps doctors look for specific physical markers that may suggest chromosomal differences, such as Down syndrome or other genetic abnormalities. This safe and non-invasive test gives valuable insights into the baby’s overall health and development.

Purpose of a Genetic Sonogram

The main goal of a genetic sonogram is early detection. It helps identify markers that can guide further testing or genetic counseling if needed. When performed at the right time, this scan offers reassurance to parents and helps doctors plan any additional care required. Early awareness also supports better pregnancy management and preparation for possible medical needs.

How the Scan Is Performed

The procedure is similar to a regular ultrasound. A transducer is gently moved over the mother’s abdomen to capture detailed images of the fetus. The sonographer checks the baby’s heart, brain, spine, and other organs. At Isha IVF Centre in Palanpur, our specialists use high-resolution ultrasound machines to ensure accurate results while maintaining comfort and safety throughout the scan.

Importance of Genetic Sonogram in Pregnancy

A genetic sonogram can detect subtle signs that standard ultrasounds may miss. It plays a key role when combined with blood tests or other genetic screenings. Together, they help confirm whether a baby has an increased risk of genetic conditions. At Isha IVF, we use this combined approach to give parents a clearer understanding of their baby’s health.