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joven embarazada de pie junto la ventana en casa portada TPNI casos especiales PLUS
joven embarazada de pie junto la ventana en casa portada TPNI casos especiales PLUS

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

810,00 €
Acude a un centro para la toma de muestra

Does your pregnancy have special characteristics and require the highest genetic coverage?
The TPNI Special Cases PLUS is the most comprehensive non-invasive prenatal test for complex pregnancies, offering a thorough analysis of chromosomal abnormalities and microdeletions with the highest accuracy.
¿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 confirmation email and an invoice in your email inbox.
2.- Visit your nearest center: with your email and/or invoice (you can show it on your phone), come to any of our Laboratorio Echevarne centers. No appointment is required.
3.- Professional sample collection: our specialized staff will take the sample quickly and safely.

Consulta tu centro más cercano →

Descripción

The NIPT Special Cases PLUS is our most comprehensive NIPT for special pregnancies: it analyzes cell-free fetal DNA in detail from the 10th week of pregnancy (16th week if there is evidence of a vanishing twin before week 8), using a simple maternal blood sample.

Suitable for:
• Singleton pregnancy · Pregnancy through egg donation
• Twin pregnancy (sex chromosome aneuploidies are not reported)
• Pregnancy with evidence of a vanishing twin before week 8 (the test is performed from week 16)

What does it detect?
• Trisomy 21, trisomy 18 and trisomy 13 · other autosomal trisomies
• Sex chromosome aneuploidies (singleton pregnancies only) · presence/absence of the Y chromosome
• 92 microdeletions/duplications >3 Mb · copy number variants (CNVs)

It is the most comprehensive and advanced non-invasive prenatal screening test available for special cases, including twin pregnancies conceived through egg donation, with over 99% reliability for the most relevant abnormalities.
Looking for even broader coverage? The Monogenic NIPT includes all the coverage of the Special Cases PLUS, in addition to the analysis of 202 monogenic diseases.

¿Is it suitable for me?

This test is for you if:
• Your pregnancy involves a special situation, whether singleton, twin, conceived through egg donation, or with evidence of a vanishing twin.
• If there is evidence of a vanishing twin before week 8, the test can be performed from week 16.
• You want a comprehensive study, even in complex genetic situations.

Descubre qué TPNI se adapta mejor a tu embarazo aquí

Sample type: Blood plasma

Go to your nearest center with your confirmation email or invoice.

Results in 8 days

Algunos centros requieren de cita previa o no realizan pruebas concretas. Consulta la disponibilidad y condiciones específicas de cada centro aquí.

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

810,00 €

Resolvemos todas tus dudas

Benefits

• Designed to address special pregnancy situations: singleton, twin, egg donation, or vanishing twin.
• Broader coverage: trisomies 21, 18, 13, T9, T16, T22, aneuploidies of other chromosomes, sex chromosome aneuploidies in singleton pregnancies, 92 microdeletions/duplications >3 Mb and CNVs >5 Mb.
• Peace of mind from the beginning of pregnancy: can be performed from week 10.
• Non-invasive: with a simple maternal blood draw, with no risk to you or your baby.
• High accuracy: more than 99% reliability in the detection of Down syndrome and other common trisomies.

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.


Before visiting the laboratory, you must first see a doctor so they can provide you with the prescription and complete the information on this document.

CLICK HERE.

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

What makes TPNI Special Cases PLUS different from other TPNIs?

It is the most comprehensive test for special pregnancies, detecting not only trisomies and sex aneuploidies but also 92 microdeletions/duplications and copy number variations (CNV).

In what types of pregnancies is TPNI Special Cases PLUS recommended?

It is recommended in singleton pregnancies, twin pregnancies, egg donation, and in cases of vanished twin before week 8 (performed from week 16 onwards).

From which week of gestation can it be performed?

Starting from week 10. In case of evidence of vanishing twin before week 8, it can be done from week 16 onwards.

Is the TPNI Special Cases PLUS test safe?

Yes, it is a non-invasive test performed with a maternal blood sample, with no risk to the mother or the fetus.

What information about sex aneuploidies is obtained in twin pregnancies?

In twin pregnancies, the test does not report sex chromosome aneuploidies; this information is only available for singleton pregnancies.

What should I do if the result indicates "High Risk"?

It is essential to consult your gynecologist. A high-risk result carries a minimal possibility of a false positive; therefore, confirmation requires a diagnostic test such as amniocentesis.

How much does the NIPT Special Cases PLUS cost?

The NIPT Special Cases PLUS costs €810. Check the other TPNI options and prices in our comparison table.

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Customer Reviews

“

The process was very simple, with just a blood draw, and the report offered a very comprehensive genetic analysis. It gave me great peace of mind to know that everything was fine. I recommend it without hesitation.

”
Manuela L.
León, León
“

The laboratory service was impeccable and the level of detail in the report, impressive: it not only detects the main trisomies but also microdeletions and chromosomal variations. It is a very comprehensive, reliable test with an accuracy that inspires complete confidence.

”
Ángela D.
Elche, Valencia