
31/07/2025
🔬 AMNIOCENTESIS
Screening for Genetic Diseases in Your Unborn Baby
When it comes to your baby’s health, early answers matter.
Amniocentesis is a safe and reliable prenatal test performed between 15 to 20 weeks of pregnancy. It helps detect genetic and chromosomal conditions in the unborn baby — so parents can make informed decisions.
What can it detect?
✅ Down Syndrome
✅ Thalassemia
✅ Neural Tube Defects
✅ Spinal abnormalities
✅ Genetic disorders
How is it done?
A small amount of amniotic fluid is drawn using a thin needle under ultrasound guidance. It’s a quick, mostly painless, daycare procedure performed by a Fetal Medicine Specialist.
💡 Amniocentesis doesn’t treat — it prepares.
Knowledge is power, and early screening empowers parents to plan better for their child’s future.
For more information and personalized care, consult us today at +91-9818852295
Visit: www.drmamtaphogat.in to know more.