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feliz joven embarazada en camiseta blanca en sala estar portada TPNI monogenicas
feliz joven embarazada en camiseta blanca en sala estar portada TPNI monogenicas

TPNI MONOGENIC (Monogenic Non-Invasive Prenatal Test)

1.550,00 €
Acude a un centro para la toma de muestra

Do you want to know your baby's health in maximum detail?
The Monogenic TPNI is a non-invasive prenatal test that assesses the risk of 202 dominant monogenic diseases, providing detailed information about your baby's health.
¿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 needed.
3.- Professional sample collection: our specialized staff will take care of the sample extraction quickly and safely.

Consulta tu centro más cercano →

Descripción

The Monogenic NIPT is a non-invasive prenatal test performed from a maternal blood sample between weeks 10 and 24 of pregnancy.

This test detects the risk of 202 dominant monogenic diseases associated with specific alterations in 155 genes. These include skeletal disorders, neurological and muscular diseases, craniosynostosis, and multisystem syndromes.

It is indicated for women with a singleton pregnancy and couples with advanced paternal age. It cannot be performed in cases of egg donor, fetal death, vanishing twin, or multiple pregnancy.

The Monogenic NIPT also includes all coverages of the Special Cases Plus NIPT, offering the most comprehensive non-invasive prenatal screening available today.

¿Is it suitable for me?

This test is for you if:
• You are pregnant from week 10 onwards.
• You have a family history of monogenic diseases.
• You want the most comprehensive genetic evaluation available.
• You are looking for screening beyond the classic trisomies.
• It cannot be performed in multiple pregnancies, egg donation cases, fetal death, or vanishing twin cases.
If you still have doubts about which NIPT modality best suits your situation, you can consult our comparison table here: 👉 Which NIPT is mine?

Sample type: Blood plasma

Includes: Voucher to attend a center for sample collection

Results in 18 days

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TPNI MONOGENIC (Monogenic Non-Invasive Prenatal Test)

1.550,00 €

Resolvemos todas tus dudas

Benefits

• Expanded coverage: detects the risk of 202 dominant monogenic diseases associated with 155 genes.
• Advanced clinical evaluation: includes neurological, muscular, skeletal, and multisystemic pathologies.
• Non-invasive: only requires a maternal blood draw.
• Includes Special Cases Plus NIPT: both coverages are combined in a single test.

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 18 business days* you will receive a notification by email and SMS.
With that notification, you will be able to 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:
Not detected: no pathogenic or likely pathogenic variant is found within the analyzed range. Confirms with 99% certainty that the fetus does not have the included diseases, although it does not rule out other alterations.
Detected: a pathogenic variant is identified in one of the analyzed genes, indicating a higher risk of being affected by the associated disease. In this case, a confirmatory diagnostic test (for example, amniocentesis) and evaluation by your gynecologist will be necessary.

How does it work?

Frequently Asked Questions

What types of diseases does the TPNI Monogenic detect?

Detects the risk of 202 dominant monogenic diseases associated with alterations in 155 genes, including skeletal and neurological disorders.

From which week of pregnancy can the Monogenic NIPT be performed?

It can be done starting from the 10th week of pregnancy.

Is the TPNI Monogenic test invasive?

No, it is a non-invasive test performed through a simple blood sample from the mother.

What benefits does the TPNI Monogenic offer?

It offers a technically superior detection of monogenic diseases, is non-invasive, and can be performed from the 10th week of pregnancy.

What does a "Not detected" result mean in Monogenic TPNI?

A result of "not detected" indicates that no relevant genetic alterations have been detected, with a very low risk of presenting any of the evaluated conditions, although it does not completely rule out a genetic alteration.

What should I do if the result says "Detected"?

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

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Customer Reviews

“

The nurse explained everything to me with great warmth and professionalism. Without a doubt, a test that provides confidence and peace of mind at such an important moment.

”
Celia L.
Tàrrega, Lleida
“

I was impressed by the number of diseases it analyzes and the clarity of the report. The process was simple and risk-free. Highly recommended for those seeking maximum accuracy.

”
Mónica A.
Tortosa, Tarragona

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