Prenatal Screening & Diagnostics
Comprehensive fetal screening and diagnostic solutions for early risk detection to support a healthy, informed pregnancy journey.
Prenatal screening and diagnostic services provide critical information about the health and development of a fetus during pregnancy. These tests help assess the risk of chromosomal conditions, structural anomalies, and inherited disorders—enabling early detection, timely intervention, and informed decision-making. Our offerings include non-invasive screening options, trimester-based risk assessments, and confirmatory diagnostic tests tailored to various stages of pregnancy.
NICC® (Non-Invasive ChromosomesCheck)
Non-invasive prenatal test (NIPT) to assess the risk of fetal chromosomal aneuploidies for:
– Trisomies: Down Syndrome (Trisomy 21), Edwards Syndrome (Trisomy 18), Patau Syndrome (Trisomy 13), Trisomy 9, 16 & 22
– Sex chromosome aneuploidies: Turner Syndrome (XO), Klinefelter Syndrome (XXY), Triple-X Syndrome (XXX), Jacob’s Syndrome (XYY)
– Other autosomal chromosomes aneuploidy
NICC® (Non-Invasive ChomosomesCheck) Extended
Non-invasive prenatal test (NIPT) to assess the risk of fetal chromosomal aneuploidies for:
– Trisomies: Down Syndrome (Trisomy 21), Edwards Syndrome (Trisomy 18), Patau Syndrome (Trisomy 13), Trisomy 9, 16 & 22
– Sex chromosome aneuploidies: Turner Syndrome (XO), Klinefelter Syndrome (XXY), Triple-X Syndrome (XXX), Jacob’s Syndrome (XYY)
– Other autosomal chromosomes aneuploidy
– 92 microdeletion / microduplication syndromes
First Trimester Screening (FTS)
Screens for Trisomy 21, Trisomy 18/13 (combined risk) using 2 biomarkers (Free βhCG & PAPP-A).
The specimen will be tested by our qualified referral lab
Second Trimester Screening / Double Test (STS)
Screens for Trisomy 21, Trisomy 18/13 (combined risk) & NTD (Neural Tube Defect) using 2 biomarkers (Total hCG & AFP).
The specimen will be tested by our qualified referral lab
Antenatal Screening
Screens for possible disorders or infections that could affect the growing fetus.
Add-on test: Glucose, Free T4, TPHA, HbA1c, Ferritin, TFT, HbEp. No fasting required UNLESS if glucose test is added. Glucose test requires 8 hours fasting.
The specimen will be tested by our qualified referral lab
ChromosomesCheck™
Rapid aneuploidy detection of T21, T18, T13, X & Y using QF-PCR method.
Karyotype
Analyzes the number and structure of all chromosomes in order to detect abnormalities using cell culture method. The specimen will be tested by our qualified referral lab
