PRENATAL COMPREHENSIVE SCREENING PANEL 1

To be used as a prenatal screen, in conjunction with chromosome analysis, to detect aneuploidy such as Trisomies 13, 18, 21, Monosomy X etc. Prenatal microdeletion test is offered as a screening test on direct or cultured amniocytes, or direct or cultured chorionic villi to detect pathogenic microdeletions involved in the following syndromes: Angelman syndrome, DiGeorge/velocardiofacial syndrome, Prader-Willi syndrome and Williams syndrome.

  • Test Type:
  • Pre-test Information:
    Sample should be taken after 15 weeks gestation
  • Report Delivery:
    Sample Daily by 4 pm; Report 4 Days
  • Components:
    0