NIPT Gender is the simplest version of the NonInvasive Prenatal Test (NIPT), designed for parents who primarily want to know their baby’s sex early in pregnancy.
NIPT Basic is the entrylevel NonInvasive Prenatal Test designed to screen for the most common chromosomal conditions in pregnancy.
NIPT Standard is a more comprehensive version of the NonInvasive Prenatal Test, designed for parents who want deeper insights into their baby’s chromosomal health.
NIPT Plus is an advanced version of the NonInvasive Prenatal Test (NIPT) designed to give expecting parents the most comprehensive view of their baby’s chromosomal health.
Covers breast, ovarian, colorectal, prostate, pancreatic, gastric, melanoma, endocrine, and more.
BRCA1/2 and related genes for breast and ovarian cancer risk.
Genes linked to inherited prostate cancer risk.
Genes associated with inherited pancreatic cancer risk.
Genes for Lynch syndrome and other colorectal risks.
Pregnancy is a journey filled with important decisions, especially regarding your baby’s health. One screening option that has become the global gold standard and is now increasingly available for NIPT in Nigeria is Non-Invasive Prenatal Testing.
Unlike traditional methods that may involve risks, NIPT uses a simple blood sample from the mother. Because it is non-invasive, it carries zero risk of miscarriage, making it the safest early screening tool for expectant parents today.
Start by exploring Syndicate Bio’s genetic testing options to see which tests are available.
NIPT is a prenatal screening test that analyses small fragments of foetal DNA circulating in the mother’s bloodstream. This test can typically be done as early as 10 weeks into pregnancy.
The main purpose of NIPT is to screen for certain chromosomal conditions, including:
Because the test examines foetal DNA, it provides more accurate screening results than many traditional blood tests.
For many families in Lagos, Abuja, and beyond, NIPT offers peace of mind through:
For parents who want additional reassurance during pregnancy, this screening can provide valuable insights.
NIPT may be particularly recommended for the following: while any pregnant woman can opt for this test, it is highly recommended for:
Pregnant women over age 35
Pregnancies with abnormal ultrasound findings
Families with a history of chromosomal conditions
Parents who want early reassurance about their baby’s genetic health
If you’re unsure whether NIPT is appropriate for your situation, you can speak with a specialist before deciding on a test.
Chat with a specialist to learn more about prenatal genetic screening
It’s important to remember that NIPT is a screening test, not a diagnostic test. A high-risk result does not confirm that a baby has a genetic condition. Instead, it indicates that further testing may be recommended.
Many families use NIPT results as a first step in understanding their baby’s health and deciding whether additional diagnostic tests are necessary.
If you’re expecting a baby and considering prenatal screening, the most important step is getting reliable information early. You can explore available prenatal genetic testing services at Syndicate Bio and learn which tests may be appropriate for you.
Your family history is a roadmap, not a diagnosis. Early awareness could make a life-saving difference for you and your loved ones.
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