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Comprehensive genetic counselling before, during and after testing - explaining what NIPT, Karyotype, FISH, Microarray, WES or Thalassemia Screening results mean for your baby, in calm, plain language.
Genetic counselling is a dedicated consultation to help you understand genetic risk, testing options, and results - before conception, after a high-risk screening result, or following an abnormal finding on a scan. Testing options include NIPT, Karyotype, FISH, QFPCR, Microarray, WES, Thalassemia Screening, Mutation Matching and Fetal Blood Grouping, each explained in the context of your specific situation.
Genetic counselling supports informed, confident decision-making at several points across the pregnancy journey.
Understanding genetic risk factors before you conceive.
Clear explanation of Double Marker / NT screening outcomes.
Guidance following a congenital anomaly or abnormality on a TIFFA scan.
Explaining NIPT, Karyotype, FISH, Microarray, WES and Thalassemia Screening in plain language.
NIPT (Non-Invasive Prenatal Testing) analyses fetal DNA in a maternal blood sample to screen for common chromosomal conditions, often recommended after a high-risk NT or Double Marker result.
Screening tests (like NIPT or the Double Marker Test) estimate risk; diagnostic tests (like Karyotype, CVS or amniocentesis-based testing) provide a definitive result, and the choice between them is discussed in counselling.
Yes - every result is discussed in a dedicated session, explaining what it means for your baby and family, and what your options are going forward.
No - pre-conceptional genetic counselling is valuable for any couple wanting to understand their genetic risk factors before or during pregnancy.
Call, WhatsApp, or request an appointment online - our care team will confirm your slot with Dr. Priyanka.