Confirmatory tests on fetal samples (amniotic fluid or chorionic villi) for chromosomal/genetic abnormalities.
At Labassure, we offer a comprehensive suite of prenatal diagnostic tests designed to provide clear, accurate, and timely answers in high-risk pregnancies or where screening tests have raised concerns. Unlike screening methods, these tests are diagnostic—meaning they can confirm or rule out genetic and chromosomal abnormalities with a high degree of certainty.
These tests are typically performed on amniotic fluid or chorionic villi samples collected via amniocentesis or chorionic villus sampling (CVS), under the guidance of a fetal medicine specialist.
Gold standard for detection of chromosomal abnormalities especially balanced translocations
Rapid assessment of specific chromosomal aberrations including translocations. Highly useful in prenatal screening and cancer diagnostic testing
High resolution genome wide screening of microdeletions/duplications and chromosomal anomalies
Rapid assessment of specific chromosomal aberrations using molecular methods.
Targeted and reliable detection of known genetic variants using gold-standard sequencing technology.
