TPNI EXTENDED (Extended Non-Invasive Prenatal Test)

• Expanded coverage: chromosomal abnormalities, triploidies, sex aneuploidies, and clinically relevant microdeletions.
• Peace of mind from the start of pregnancy: can be performed from week 9 onwards.
• Non-invasive: with a simple maternal blood draw, no risks for you or the baby.
• Technically superior: detects conditions that other tests do not identify, such as molar pregnancy, triploidy, or vanishing twin.
• Unique in differentiating the genetic profile: the only test that distinguishes between maternal and fetal DNA, reducing false positives and false negatives.
• High accuracy: over 99% reliability in detecting Down Syndrome and other common trisomies.

The purchase of this test is a voucher for taking the test at a Laboratorio Echevarne branch.

Fasting is not required.

It is recommended to eat something 30 minutes before the analysis.

Extractions available Monday to Friday (except on the eve of public holiday Fridays).

A medical request is mandatory to perform this test.

Your results, clear and accessible:
Within 8 business days* you will receive a notification by email and SMS.
With that notification, you can access and download your report from our online Patient Portal.
*Delivery time may occasionally be extended due to technical needs.
Once you have your report, consult a healthcare professional who can interpret it with you and, if necessary, create a personalized action plan.

Interpretation of the results:
Low risk: confirms with 99% certainty that the fetus does not have the analyzed syndromes, although it does not rule out 100% other alterations.
High risk: it is essential to consult your gynecologist. Confirmation requires a definitive diagnostic test, such as amniocentesis.

In addition to common trisomies, the EXTENDED NIPT detects important microdeletions such as 22q11.2, Monosomy 1p36, Cri-du-Chat Syndrome, Prader-Willi Syndrome, Angelman Syndrome, and Triploidy.

No, the EXTENDED NIPT is indicated only for singleton pregnancies and is not available for twin pregnancies or egg donation pregnancies.

It is done through a simple blood draw from the mother, making it a safe and non-invasive method for the fetus.

Results are usually available within 8 business days, although sometimes the timeframe may be extended due to technical requirements.

A "Low risk" result indicates that the fetus has a 99% chance of not having the analyzed syndromes, although it does not completely rule out chromosomal abnormalities.

Yes, to carry out this test it is necessary to have a medical request.