NABL Accredited
Detection of Fetal Aneuploidies (13, 18, 21 and XY) by QF PCR and Chromosomal Array CGH, Amniotic Fluid
Sample Collection & Prep:
Amniotic Fluid (15-20 ml) in a sterile screw cap tube
Specimen Type:
Amniotic Fluid
Testing Methodology:
Array Comparative Genomic Hybridization (Array CGH) 20-30 ML
Testing Schedule:
Mon–Sat 15th day
Report Delivery:
Within 5th day via WhatsApp & Email
Fasting Requirement:
No strict fasting required before sample collection
Quality Standard:
100% NABL Accredited clinical reference laboratory testing
Clinical Instructions:
Sample stable for 1 day at Ambient temperature and 3 Days at 2 to 8 degree celsius. Sample to be preferably shipped at Referigerated condition • 3-5 ml EDTA Blood sample of Mother is mandatory. Sample stable for 3 Days at Amibent Temperature and 7 Days at 2 to 8 degree celsius .Completely filled TRF along with detailed clinical history, Ultra Sound report (USG), Dual and Quadruple Marker Report. Duly signed consent form (Form G) as per PCPNDT, Refering Drs prescription
₹18000
Test Information
Preparation requirements and diagnostic clinical parameters.
Parameters
1 Parameter- 1 diagnostic parameter
- Automated calibrated clinical analyzer
Fasting & Prep
No Fasting- No strict fasting required
- Plain drinking water intake permitted
Specimen
Amniotic Fluid- Matrix: Amniotic Fluid
- Prep: Amniotic Fluid (15-20 ml) in a sterile screw cap tube
Turnaround
5th day- Report in Mon–Sat 15th day
- Verified PDF via WhatsApp & Email
Detection of Fetal Aneuploidies (13, 18, 21 and XY) by QF PCR and Chromosomal Array CGH, Amniotic Fluid
1 parameter across 1 body system
Blood & Hematology Health
Analyzes blood cells, hemoglobin levels, and cellular health markers.
1 Parameter
Detection of Fetal Aneuploidies (13, 18, 21 and XY) by QF PCR and Chromosomal Array CGH, Amniotic Fluid
Detection of Fetal Aneuploidies (13, 18, 21 and XY) by QF PCR and Chromosomal Array CGH, Amniotic Fluid
