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Known as
Known as :
Lysozyme, Serum
Related Test Group
Related Test Group :
Cancer Screening
Oncology
ImmunoChemistry
MicroSeq+\ 16S/ITS Metagenomics with research report
0
AED
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MicroSeq+\ 16S/ITS Metagenomics with research report
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Related Test Group
Related Test Group :
Molecular Diagnostic
Microbiology
MicroSeq\ 16S/ITS Metagenomics
0
AED
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MicroSeq\ 16S/ITS Metagenomics
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Related Test Group
Related Test Group :
Molecular Diagnostic
Microbiology
Microalbumin, 24 hour Urine
0
AED
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Microalbumin, 24 hour Urine
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Known as
Known as :
24 Hour Urine Microalbumin
Microalbumin - Quantitative (24 hour Urine)
Microalbuminurea (24 h Urine)
Albumin, 24 Hour, Urine
Albumin Quantitative Urine 24H
Microalbuminuria (24 h Urine)
Micro-albumin, 24 H Urine
Related Test Group
Related Test Group :
ImmunoChemistry
Diabetes Tests
Kidney Tests
Protein in Urine (Proteinuria)
Kidney Disease
Urology
NIPT
100
AED
CPT: 123432
Results in 1
Days
Read more
NIPT
Non-Invasive Prenatal Testing (NIPT) is a modern genetic screening method that analyzes cell-free fetal DNA (cffDNA) circulating in the mother’s blood. It is performed as early as the 10th week of pregnancy and provides valuable information about the risk of chromosomal abnormalities in the fetus.
NIPT is important for:
• Early detection: Identifies common chromosomal conditions such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13) at an early stage of pregnancy.
• Non-invasive: Requires only a maternal blood sample, avoiding the risks associated with invasive procedures like amniocentesis or chorionic villus sampling (CVS).
• High accuracy: Offers very high sensitivity and specificity for common trisomy’s compared to traditional biochemical screening tests.
• Broader scope: it can also screen for sex chromosome abnormalities (Turner, Klinefelter, Triple X, XYY) and sometimes microdeletions.
• Guides clinical decisions: Helps families and healthcare providers decide whether further diagnostic testing is needed.
NIPT is an early, safe, and accurate way to check the baby’s DNA for certain genetic conditions. It helps parents feel more informed and prepared, but it is always followed by confirmatory tests if results show high risk.
Biomarkers
Biomarkers
Susceptibility / Risk Biomarkers
cell-free fetal DNA
cffDNA
Related Test Group
Related Test Group :
Hematology
Blood Bank
Blood Type & Blood Disorder Tests
Blood Type
General Health Tests
New Born Screen
Prenatal testing
Aneuploidy Screening
Neonatal Bilirubin, Serum
0
AED
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Neonatal Bilirubin, Serum
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Known as
Known as :
Bilirubin Neonatal, Serum
Related Test Group
Related Test Group :
Clinical BioChemistry
Liver Tests
Hepatic Function
Liver Disease
New Born Screen
New Test
2
AED
CPT: 3214r
Results in 2
Days
Read more
New Test
wdefrgvb
Symptoms
Symptoms
Symptom Category 1
Symptom 1 2
Conditions
Conditions :
The analysis requires a 12-hour fast.
Known as
Known as :
TEST
Related Test Group
Related Test Group :
Acidosis & Alkalosis
Adrenal Fatigue Tests (Hormone)
OncoSeq:BRCA
0
AED
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OncoSeq:BRCA
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Related Test Group
Related Test Group :
Molecular Diagnostic
Cancer Screening
Breast Cancer
Oncology
OncoSeq:BRCA+ with clinical report
0
AED
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OncoSeq:BRCA+ with clinical report
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Related Test Group
Related Test Group :
Molecular Diagnostic
Cancer Screening
Breast Cancer
Oncology
Parvovirus B19, Molecular Detection, PCR, Plasma
0
AED
Read more
Parvovirus B19, Molecular Detection, PCR, Plasma
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