Prenatal Diagnostic Facilities & Services
Our patients benefit from our expertise and advanced technology, including Nuchal Translucency (NT) screening, a new, non-invasive test provided at only a few centres nationwide performed early in pregnancy to indentify increased risk for Down syndrome and other birth defects.
Our Specialized Services include:
- Nuchal Translucency screening for Chromosomal anomalies
- Chromosomal Analysis (Karyotyping) from:
- Chorionic Villus Sampling (CVS)
- Amniocentesis – Triple Market Test
- Cordocentesis
- Foetal Blood Transfusion in Rh isoimmunised Pregnancies
- Complete Evaluation of Recurrent Pregnancy Miscarriage
- Foetal Biophysical Profile
- Foetal Echo-Cardiography
- Genetic Counseling
- Foetal Reduction
Cytogenetics and Molecular Diagnostic Services
- Fluorescence In-Situ Hybridization (FISH)
- Molecular Diagnosis using PCR Technique (Polymerase Chain Reaction)
- Duchenne Muscular Dystrophy (DMD)
- Sickle cell Disease
- Thalassemia Screening and Diagnosis
- Y-Chromosome Micro Deletions
- Preimplantation Genetic Diagnosis (PGD)