NIPT Microdeletion – Advanced

Description

NIPT Microdeletion – Advanced is a prenatal screening test that not only detects common chromosomal abnormalities like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18) and Patau syndrome (Trisomy 13) but also identifies rare microdeletion syndromes such as DiGeorge syndrome (22q11.2 deletion), Prader-Willi syndrome and Williams-Beuren syndrome. This non-invasive test analyzes fetal DNA from the mother’s blood as early as the 10th week of pregnancy, providing detailed insights into the baby’s genetic health with high accuracy and without the risks of invasive procedures.