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/cultured amniocytes or direct/cultured chorionic villi to detect pathogenic microdeletions involved in the following syndromes: Angelman syndrome, DiGeorge/Velocardiofacial syndrome, Prader-Willi syndrome and Williams syndrome.
Parameter(s) covered : 7
Report Frequency: Sample Daily by 4 pm; Report 4 Working days
Special Instruction: Sample should be taken after 12 weeks gestation. Duly filled Prenatal Genetic Testing Consent Form (Form 60) is mandatory. Samples shall be accepted only from registered genetics clinics under PCPNDT Act.
Price : ₹ 11900.00
Parameters
- Chromosome 13 (Patau syndrome)
- Chromosome 15q11-q12 (Prader-Willi / Angelman)
- Chromosome 18 (Edwards syndrome)
- Chromosome 21 (Down syndrome)
- Chromosome 22q11.2 (Di-George)
- Chromosome 7q11.2 (William-Beuren)
- Sex chromosomes*