Importance of Genetic Testing During Pregnancy | Dr. Sunil Kumar G S

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Pregnancy is a journey filled with joy and anticipation, but sometimes, ultrasound scans reveal unexpected findings in the baby. These findings could indicate potential chromosomal or genetic abnormalities.

✨ To provide clarity, we may recommend diagnostic tests like:
➡️ Amniocentesis or CVS (Chorionic Villus Sampling), where small samples of amniotic fluid or tissue are collected.

These samples allow us to perform advanced tests like:
🔬 FISH
🔬 Karyotyping
🔬 Microarray
🔬 QF-PCR
🔬 Clinical Exome Sequencing

These tests give a detailed understanding of the baby’s genetic makeup, helping parents make informed decisions.

💡 Many mothers also ask about Double Marker, Quadruple Marker, and NIPT blood tests. While these are excellent screening tests, it’s essential to remember they don’t provide a definitive diagnosis.

As a fetal radiologist, my goal is to guide you through this process and help you understand the significance of these tests in ensuring the health and well-being of your baby.

🩷 Empowering parents, one step at a time!

👉 If you have questions about genetic testing or need guidance on your pregnancy journey, drop your queries in the comments or send me a DM. Let’s ensure you feel supported every step of the way!

#PregnancyCare #FetalMedicine #GeneticTesting #PrenatalCare #ExpectingMoms #HealthyBaby #addonscansandlabs
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