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Non Invasive Prenatal Test Plus

Detects Down, Edwards, Patau, Turner syndromes, the future sex of the baby, and many other abnormalities and conditions from week 10. With 99% accuracy.

Are you pregnant and want to know that everything is fine with your baby? From week 10 of gestation, the "Non Invasive Prenatal Test PLUS" will allow you to know if your baby is developing any trisomy or more common alterations that can be serious.

Non Invasive Prenatal Test Plus

Price: 720.00€

Price with discount: 590,00€

Service Description:

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Get the peace of mind of knowing that your future baby is in perfect health. This test will allow you to rule out Down syndrome (trisomy 21), Edwards (trisomy 18), Patau (trisomy 13), Turner (Monosomy X), and many other abnormalities and conditions. You also have the option to know the gender of your future baby if you wish.

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The report explains in a simple way if there is a low, medium or high risk that your baby will develop any of these syndromes during pregnancy.

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Results available within 6 business days from receipt of the sample at the laboratory. Official results. No prior medical prescription is required.

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The test is carried out through a blood sample from the mother from the 10th week of pregnancy, so it does not represent any risk for the fetus or the mother.

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This test can be done from week 10 of pregnancy.

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Receive a genetic counseling appointment for the explanation of your results, at no additional cost. (This service is optional).

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Rod Paley


Graeme McKenzie


Daniel Crigan


Our partner labs, nationally and internationally certified

Imegen Health Code
Quiron Salud

We put at your disposal more than 150 extraction points, the largest network in Spain.

Why is this analysis useful for me?

  • It allows you to detect the presence of genetic markers in the fetus of Down, Edwards, and Patau syndromes at an early stage of pregnancy.
  • You can avoid invasive tests like amniocentesis, which are uncomfortable for both mother and baby.
  • Allows you to take decisions based on the current legislation.

Who should have this test?

  • It will provides you peace of mind about your pregnancy about your pregnancy from week 10.
  • Superior accuracy (less than 0.1% false positives).
  • If you had previous pregnancies with the presence of trisomies.
  • If it is your first pregnancy and you are over 35 years old.
  • If you have fetal ultrasound abnormalities.
  • If you have a high hereditary risk of fetal aneuploidies.

What is a non-invasive prenatal test (NIPT)?

  • The Non-invasive Prenatal Test is a maternal blood test that detects the main chromosomal alterations of the baby, avoiding the possible risks of amniocentesis.
  • When you are pregnant, your blood contains fragments of your child's DNA. This test has greater accuracy and a lower rate of false positives; compared to traditional invasive tests.

What technology does it use?

  • Analyze specific chromosome fragments using Next Generation Sequencing (NGS) technology.
  • It is a highly precise quantification technique with a sensitivity and specificity greater than 99%.
  • The test is validated for use in single and twin pregnancies and IVF (own egg or egg donation).


    Analysis of numerical chromosomal alterations (trisomies and monosomies) and structural alterations (deletions and duplications) of a molecular size equal to or greater than 7 Mb of all autosomes (from chromosome 1 to 22), sex chromosomes (X and Y) and determination of fetal sex.

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How the test works

  1. elige tu test genético
    Purchase your service online with a discount to get a voucher.
  2. frotis bucal para análisis
    Go to an extraction centre with your voucher.
  3. instrucciones de uso
    One of our partner labs makes the analysis.
  4. instrucciones de uso
    You receive the results by email.

You can help by sharing this information with your contacts or doctor

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