PrenatalSafe is a non-invasive test analysing foetal DNA to detect chromosomal abnormalities and genetic conditions. Offering 9 CE-IVD levels of investigation, it can identify aneuploidies, structural chromosomal abnormalities such as microdeletions and microduplications, and both de novo and inherited genetic conditions. With a sensitivity and specificity of over 99%, the test provides an accurate assessment with no risk to the developing foetus.
RhSafe Test
RhSafe detects the presence or deletion of the RHD gene (fetus RhD+) in RhD-negative mothers using real time PCR for exons 5 and 7.
Microdeletions
Screens for microdeletions associated with several genetic syndromes, including DiGeorge, Prader-Willi, Angelman, and Jacobsen’s syndrome.