Includes: 1 test
hCG, AFP, UE3, Quick Precise Reports, Reporting as per NABL ISO guidelines, Free Home Sample Collection, Free Doctor's Consultation
A. It’s a simple test available at a nominal Triple Marker Test Price and is recommended for pregnant women to determine any genetic or chromosomal disorders developed during the prenatal phase.
A. It is like any other blood test and requires no special preparation or fasting. During the examination, your healthcare provider will clean the skin, ask you to make a fist to make the vein more accessible, insert the needle to draw some blood specimens, and collect them in a vial to send to the lab for analysis.
A. It’s a screening test and not a diagnostic test and can only predict any possible abnormalities or genetic disorders in a baby. There are chances of false results. Therefore, doctors can prescribe several other scans or diagnose if required for better clarity or accuracy.
A. It can detect Trisomy 18, Down syndrome, Neural tube defects, and other Chromosomal abnormalities in a fetus to begin the treatment as soon as possible.
A. Blood is drawn from the mother only. Therefore, no such risk to the baby is involved in the procedure.
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