The NIPT Genetic Package detects chromosomal disorders in the fetus at early stages.
The NIPT Genetic Package offers you a proactive opportunity to ensure your fetus’s health through an accurate, non-invasive test performed in the early stages of pregnancy. The NIPT genetic test relies on analyzing fetal DNA found in the mother’s blood to identify any chromosomal disorders, such as Down syndrome, Edwards syndrome, Patau syndrome, and other chromosomal abnormalities that may affect fetal development.
This test is completely safe for the fetus and does not require any surgical intervention.
It is performed starting from the tenth week of pregnancy. The NIPT genetic test is particularly suitable for those who are pregnant over the age of 35, have a family history of genetic conditions, or have abnormal ultrasound results.
This test is considered a smart step to prevent unexpected health surprises, as it provides you with reliable results with high accuracy, helping you make medical and psychological decisions with confidence and awareness from the beginning of pregnancy.
The test is performed only once during pregnancy, but it provides you with essential information that significantly impacts your journey as a mother. If you wish to experience a more comfortable and reassuring pregnancy, the NIPT Genetic Package is your ideal choice to ensure a healthy start to your child’s life.
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