NIPT extended panel

5 500 000 UZS

This test detects the following anomalies in the fetus: trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), trisomy 13 (Patau syndrome), sex aneuploidies; microdeletion syndromes: microdeletion 22q11.2 (DiGeorge syndrome), microdeletion 1p36 (1p36 syndrome), microdeletion 15q11-13 (Angelman/Prader-Willi syndrome), microdeletion 4p16.3 (Wolf-Hirschhorn syndrome), microdeletion 5p15 (cri-du-chat syndrome); when carrier status of autosomal recessive diseases is detected in the pregnant woman's gene: CFTR, PAH, GALT, GJB2, SLC26A4, TPP1, ATP7B, DARS2, DHCR7, HEXA, IDUA, PIGN, PKHD1, PMM2, SLC26A2, USH2A, SMARCAL1, ALDOB. Turnaround time: 10 working days.