PRENATAL HEMOPHILIA A

This test screens for genetic mutations associated with Hemophilia A in a fetus. It is used to diagnose or rule out this bleeding disorder in an unborn child.

Also known asPrenatal Hemophilia A Prenatal Hemophilia A

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

12 Working Days

Test details
Preparations

No special preparations needed

Test included
PRENATAL HEMOPHILIA A includes 1 parameter

  • Prenatal Hemophilia A

Test code

G503

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Amniotic FluidPlain Sterile Vaccutainer 3 ML
Peripheral BloodOthers3 ML

Specimen stability information

Amniotic Fluid, Peripheral Blood

Specimen rejection criteria

Test run frequency

Every Day TIME - 08:00

Turn around time

12 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

PRENATAL HEMOPHILIA A

16500