You checked their heartbeat. You counted their fingers and toes. You made sure they were feeding and sleeping well.
There's one more thing you can know.
What their DNA may be telling you — before symptoms ever do.
Some genetic conditions stay silent at birth.
No signs. No symptoms. Neonatal genomic testing can help identify certain hidden risks early — giving you and your doctor the chance to monitor, prevent complications, and plan ahead.
Because your baby deserves more than a healthy beginning.
They deserve every chance at a healthy future.
Know early. Act early. One test, an early map of their health.
₹50,000, once for a map of their health that lasts a lifetime.
Talk to your doctor or genetic counsellor to understand whether genomic testing is right for your newborn.