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Genetics And Fetal Medicine
Genetics and Fetal Medicine is a specialized branch of medicine focused on diagnosing, managing, and preventing genetic disorders and fetal abnormalities during pregnancy. It combines the expertise of clinical genetics, prenatal diagnostics, and maternal-fetal medicine to ensure the healthiest possible outcomes for both the mother and baby.
Core Services Offered
1. Genetic Counseling
Risk assessment for inherited conditions
Carrier screening and interpretation of genetic reports
Support for couples with family history of genetic disorders, infertility, or recurrent pregnancy loss
2. Prenatal Diagnosis
Ultrasound-based screening (NT scan, anomaly scan)
Non-invasive prenatal testing (NIPT) for Down syndrome and other chromosomal conditions
3. Fetal Therapy & Interventions :In-utero treatment for conditions like:
Twin-Twin Transfusion Syndrome (TTTS)
Fetal anemia (intrauterine transfusion)
Fetal growth restriction
Fetal malformations amenable to early intervention
4. Newborn Genetic Testing
Chromosomal analysis (karyotyping)
Whole exome or genome sequencing for early diagnosis
Neonatal metabolic screening
Multidisciplinary Approach
The department works in collaboration with:
Obstetricians
Neonatologists
Pediatric geneticists
Radiologists
Pediatric surgeons
IVF and infertility specialists
Who Should Visit This Department?
Couples planning a pregnancy with a family history of genetic disease
Women over age 35
Parents who have experienced miscarriages, stillbirths, or previous children with birth defects
Families seeking clarity on genetic test results
???? Why It’s Important
The department bridges the gap between genomic science and maternal-fetal care, offering personalized, ethical, and compassionate services to ensure the healthiest outcomes for both mother and baby.