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TPNI SPECIAL CASES (Non-Invasive Prenatal Test Special Cases)

580,00 €
Acude a un centro para la toma de muestra

Does your pregnancy have a special circumstance and you want to have information about your baby's health? The TPNI Special Cases is a non-invasive prenatal test indicated for specific clinical situations, such as twin pregnancies from egg donation, pregnancies with vanishing twin, or pregnancies after a recent bone marrow transplant. It detects common trisomies and the presence/absence of the Y chromosome.

¿Where is it done?

We explain how it works, it's very simple:
1.- Buy your test online: once the payment is completed, you will receive a voucher in your email.
2.- Go to your nearest center: with your voucher (you can have it on your phone), come to any of our Laboratorio Echevarne centers. No appointment is necessary.
3.- Professional sample collection: our specialized staff will take care of the sample extraction quickly and safely.

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Descripción

The Special Cases NIPT is a non-invasive prenatal test performed with maternal blood from the 10th week of pregnancy. It is specifically designed for special clinical situations.

It is recommended in cases of:

-Twin pregnancy from egg donation.
-Pregnancy with evidence of vanished twin (from the 16th week).

What does it detect?
-Trisomy 21. Down syndrome
-Trisomy 18. Edwards syndrome
-Trisomy 13. Patau syndrome
-It also reports on the presence or absence of the Y chromosome.

It is a safe, reliable, and non-invasive test that helps reduce the need for risky procedures such as amniocentesis.

¿Is it suitable for me?

This test is for you if:
• You are pregnant in specific situations such as twin pregnancy by egg donation or vanishing twin.
• You want a prenatal assessment tailored to these circumstances.
• You are looking for a safe and highly accurate option in complex cases.
If you still have doubts about which NIPT modality best suits your situation, you can check our comparative table here: 👉 Which NIPT is mine?

Sample type: Blood plasma

Includes: Voucher to attend a center for sample collection

Results in 8 days

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TPNI SPECIAL CASES (Non-Invasive Prenatal Test Special Cases)

580,00 €

Resolvemos todas tus dudas

Benefits

• Recommended for complex clinical situations: twin pregnancies from egg donation or vanishing twin.
• Peace of mind from the start of pregnancy: you can perform it from week 10 onwards.
• Non-invasive: with a simple maternal blood draw, no risks for you or the baby.
• High accuracy: over 99% reliability in detecting Down Syndrome and other common trisomies.
• Versatility: suitable for single pregnancies, egg donation, or twins.

Prepare yourself

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.

Results

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.

How does it work?

Frequently Asked Questions

For what type of pregnancies is the TPNI Special Cases indicated?

It is indicated for twin pregnancies by egg donation or pregnancies with vanishing twin (from week 16 onwards).

From which week of pregnancy can this test be performed?

It can be done from the 10th week of pregnancy. 16 weeks in case of vanishing twin.

What anomalies does the TPNI Special Cases detect?

Detects Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards Syndrome), Trisomy 13 (Patau Syndrome) and reports on the presence/absence of the Y chromosome.

Is it an invasive test?

No, it is a non-invasive test performed with a maternal blood sample, minimizing any risk to the mother and the fetus.

What benefits does the TPNI Special Cases offer?

It offers high accuracy, is technically superior for detecting specific conditions in special cases, and is non-invasive, providing peace of mind to parents.

What should I do if the result is "High risk"?

If the result indicates "High risk," it is essential to consult your gynecologist to consider performing a definitive diagnostic test.

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Customer Reviews

The process was simple and risk-free, and the results came quickly with very clear explanations. It gave me a great deal of peace of mind. Totally recommendable.

Verónica X.
Palma de Mallorca, Balearic Islands

The service at the laboratory was impeccable, and the report very thorough. I felt safe and supported at all times.

Paula O.
Cádiz, Cádiz