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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 TPNI Special Cases PLUS is a non-invasive prenatal test designed to analyze fetal DNA in detail from the 10th week of pregnancy, through a simple maternal blood draw.

It is suitable for:
-Single pregnancy
-Oocyte donation pregnancy
-Twin pregnancy (does not report sexual aneuploidies)
-Pregnancy with evidence of vanishing twin before week 8 (the test is performed from week 16)

What does it detect?
-Trisomy 21. Down syndrome
-Trisomy 18. Edwards syndrome
-Trisomy 13. Patau syndrome
-Other autosomal trisomies
-Sexual aneuploidies (only in single pregnancy)
-Presence/absence of Y chromosome
-92 microdel/dup >3Mb
-CNV

It is the most complete and advanced non-invasive prenatal screening available for special cases, providing peace of mind and avoiding invasive procedures such as amniocentesis, always with an accuracy greater than 99% for the most relevant anomalies.

¿Is it suitable for me?

Este test es para ti, si:
•Tu embarazo presenta una situación especial, ya sea único, gemelar, por ovodonación, o con evidencia de gemelo evanescente.
•En caso de evidencia de gemelo evanescente antes de la semana 8, puede realizarse desde la semana 16.
•Quieres un estudio completo, incluso en circunstancias genéticas complejas.

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

• The TPNI Special Cases PLUS is designed to address special pregnancy situations.
• Suitable for: singleton pregnancy, twins, egg donation, or with vanishing twin.
• Broader coverage: analyzes trisomies 21, T18, T13, T9, T16, T22, aneuploidies of other chromosomes, sex aneuploidies in singleton pregnancy, 92 microdeletions/duplications >3Mb and CNVs >5Mb.
• Peace of mind from the start of pregnancy: can be performed from week 10.
• 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 singleton 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.


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, sexual aneuploidies are not reported with this test.

¿Cuánto cuesta el TPNI Casos Especiales PLUS?

El TPNI Casos Especiales PLUS tiene un precio de 810€. Consulta el resto de modalidades y precios de la gama TPNI en nuestra tabla comparativa.



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

If the result is "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 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