Genetic Counselling
Personalised risk assessment and counselling for chromosomal and genetic conditions.
01 · What Is This Scan
Understanding Your Risk, Clearly.
Genetic counselling is a dedicated consultation for families with chromosomal risk factors — high NT results, family history, previous affected pregnancy, or advanced maternal age. We discuss NIPT, CVS and amniocentesis options and interpret results together.
02 · Why It Matters
- Clear, unhurried explanation of risk
- Guidance on non-invasive vs invasive testing
- Support through decisions that matter
03 · What We Check
A Systematic, Head-To-Toe Assessment.
Pedigree and family history
Prior test results interpretation
Options: NIPT, CVS, amniocentesis
Post-test counselling
04 · How It's Done
Your Visit, Step By Step.
Detailed History
Three-generation pedigree taken.
Risk Review
All available results interpreted.
Options Discussion
Every test option explained.
Written Summary
Take-home summary of the discussion.
05 · Preparation
How To Prepare.
- Bring all prior scan and blood reports
- Family history of any medical conditions
- Time — please don't rush this consultation
A Note From Dr. Archana
"Genetic counselling is not about pushing a test. It is about helping you understand your situation and make the decision that is right for your family."
Dr. Archana · Fetal Medicine Specialist
06 · FAQs
Common Questions About The Genetic Counselling.
Is NIPT better than amniocentesis?
NIPT is a screening test; amniocentesis is diagnostic. They serve different purposes and we help you choose the right one for your situation.
Book Your Genetic Counselling Today.
Reports are handed to you before you leave — or on WhatsApp within the hour.