A miscarriage refers to the loss of a single pregnancy, usually occurring before the 24th week of gestation. It is relatively common, with approximately 15-20% of pregnancies ending in miscarriage. Recurrent pregnancy loss (RPL), on the other hand, is diagnosed when a woman experiences two or more consecutive miscarriages. Unlike a single miscarriage, RPL in pregnancy indicates the possibility of underlying issues that require further investigation through RPL testing.
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India's Leading NIPT Test
What is the NIPT Test for Pregnancy?
The NIPT test in pregnancy, or Non-Invasive Prenatal Testing, is a highly accurate screening tool used to detect chromosomal abnormalities in a fetus. This blood test analyses small fragments of fetal DNA circulating in the mother's bloodstream, checking for conditions like Down syndrome (Trisomy 21), Edwards’ syndrome (Trisomy 18), and Patau syndrome (Trisomy 13). MedGenome’s NIPT test in India is a safe alternative to invasive diagnostic methods and can be done as early as the 10th week of pregnancy. The results offer over 99% accuracy, providing early insights into fetal health.
Demographics
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1/200Births
Incidence of Chromosomal disorders
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13,000Births
Chromosomal abnormalities are over
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1/850 Births
Incidence of Down Syndrome
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1/1000 Births
Births with Microdeletions
Accuracy
MedGenome’s Non-Invasive Prenatal Testing excels with 99.9% accuracy, high sensitivity/specificity, low false positives/negatives, and is the only NIPT Pregnancy Test validated on the Indian population. It offers genetic counselling and fast reporting from a CAP-accredited lab in India.
Specifications
- Panel Coverage: Screens the entire fetal genome (including common aneuploidies and sex chromosome abnormalities)
- Sensitivity: 99.9%
- Specificity: 99.9%
- Drugs Tested: 18+
- Sequencing Method: Uses Next Generation Sequencing (NGS) technology
- Turnaround Time: Less than or equal to 7 working days
The conditions that our 3 tests detects
Reproductive Genetics NIPT
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Trisomy 21 (Down Syndrome)
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Trisomy 18 (Edwards’ Syndrome)
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Trisomy 13 (Patau syndrome)
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Turner Syndrome (Monosomy X/XO)
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Klinefelter Syndrome (XXY)
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Triple X (XXX)
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Jacob’s Syndrome (XYY)
Reproductive Genetics NIPT Twins
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Trisomy 21
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Trisomy 18
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Trisomy 13
Reproductive Genetics NIPT Advanced
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Rare Autosomal Aneuploidies (RAA) include trisomies in chromosomes other than 21, 18 and 13 and monosomies in all 22 chromosomes.
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Claria NIPT Advanced screens for RAAs in addition to Trisomy 13, 18, 21 and sex chromosomes.
Key Highlights of MedGenome Labs Recurrent Pregnancy Loss Test
Highly Sensitive Detection 1
Detects chromosomal deletions and duplications using a highly sensitive platform with over 99% sensitivity. 1
Highly Sensitive Detection 2
Detects chromosomal deletions and duplications using a highly sensitive platform with over 99% sensitivity. 2
Highly Sensitive Detection 3
Detects chromosomal deletions and duplications using a highly sensitive platform with over 99% sensitivity. 3
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