Fetal Medicine Centre
Advanced Prenatal Diagnosis & Fetal Care
Our Fetal Medicine Centre offers specialized care for monitoring fetal growth and detecting abnormalities during pregnancy.
- Viability and Dating Scan (8-9 weeks)
- First trimester Nuchal translucency scan (11-13+6 weeks)
- Fetal aneuploidy Screening (Trisomy 21/Down's Syndrome, T18, T13 screening)
- Preeclampsia Screening
- Early Anomaly Scan (16-18 weeks)
- Anomaly Scan/Level IScan/Targeted Imaging For Fetal AnomaliesTIFFA SCAN) 19-20 weeks
- 3D/4D Ultrasonography
- Fetal Echocardiography
- FETAL REDUCTION
- Fetal Neurosonography
- Diagnosis and management of small and growth-restricted fetuses
- Management of multiple pregnancies and their complications
- Diagnosis and Management of Fetal anaemia in Rh negative pregnancy and fetal infections
- Prediction and prevention of preterm labour
Diagnostic Procedures
- Amniocentesis
- Chorionic Villous Sampling (CVS)
- Cordocentesis (Fetal Blood Sampling)
- Diagnostic Amnioinfusion
Therapeutic Procedures
- Fetal Reduction in Multifetal gestations
- Fetal Blood Transfusion
- Amnioreduction
- Fetal Shunt Procedures
Genetic Services
- Genetic counselling and Tele-genetic counselling with clinical geneticist.
- Fetal CGH Microarray analysis, QF-PCR and FISH analysis.
- Prenatal diagnosis of genetically inherited diseases such as Thalassemia, Sickle cell anaemia, Spinal muscular atrophy, Inborn errors of metabolism (IEM), Mitochondriopathies and single gene disorde
- Molecular work up of index case (previously affected child)
- Familial genetic studies (molecular workup) for recurrent genetic disorders in the family.
Biochemical /Blood Tests Related to Fetal Medicine
- First trimester combined risk assessment of aneuppidies (Nuchal translucency & dual markers (BHCG + Papp-A).
- First trimester preeclampsia screening.
- Non invasive prenatal screening (NIPS).
- Second Trimester quadruple risk assessment for anessploidies.
- Thalassemia and Sickle cell anaemia screening