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  1. medmesafe
  2. Trisomy 21

Non-invasive prenatal test trisomy 21

Detects Down syndrome and fetal sex from the 10th week of pregnancy

Analyze the DNA of your child that you carry in your own blood to identify the presence of genetic markers of Down syndrome with great reliability and, if you wish, the sex of your baby. All with a simple analysis whose result will be explained by an expert in genetics. For the extraction you will have the largest network of laboratories in Europe.
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Week 10
From the tenth week of gestation

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99'9%
The analysis is almost 100% reliable(1)

so you can trust that the result will be accurate.

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0 risk
Non-invasive analysis

It only requires a blood sample and has no danger to the baby.

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6 - 9 days
T21 is a very fast service

which offers the answers you are looking for in a few days for your tranquility and relaxation.

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+50
We have more than 50 collaborating centers

where to perform the blood draw without an appointment.

(1) Source: Ont Health Technol Assess Ser. 2019; 19(4): 1–166.”
Non-invasive prenatal test trisomy 21
  • Detection of Down syndrome (trisomy 21)
  • You will have the option of knowing the sex of the future baby if you wish.
  • You can go to any of our more than 50 collaborated centers without prior appointment and without having to go on an empty stomach.
icono de tiempo 6 - 9 days
icono de mundo Spain
icono de la muestra Blood
icono de genes Next Generation Sequencing
icono de tiempo
  • Business days from receipt of the sample in the Laboratory
icono de mundo
  • Only available in Spain at the moment
icono de la muestra
  • Sample of blood drawn at an extraction center.
icono de genes
  • An analysis of the fetal DNA contained in the blood of the mother is performed via massive fetal genome sequencing using the Next Generation Sequencing technique.
  • This test is only for singleton gestations.
  • Indicated for pregnant women of advanced age (+35 years).
175 € *
Buy
* Up to 10% cheaper than lab fee
Access the most extensive and reputable laboratory network
elige tu test genético ⌖ More than 50 centers in Spain
○ To perform the extraction, it is not necessary to go on an empty stomach
elige tu test genético
⌖ More than 50 centers in Spain
○ To perform the extraction, it is not necessary to go on an empty stomach
A Coruña
Coruña
(A Coruña)
⌂ C/ Cuesta De La Palloza 3, 1º Izq
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Albacete
Albacete
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⌂ C/ Perez Galdós, 7 - 9
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Asturias
Gijón
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⌂ C/ Moros, 2 1ºa
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Oviedo
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Ávila
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⌂ Avenida De Portugal, 37
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Zafra
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⌂ Rambla De Catalunya, 120
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⌂ AVDA.PRINCIPE DE ASTURIAS 21-22 BAJO
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Comparison of non-invasive prenatal tests

Trisomy 21
Trisomy 18
Trisomy 13
Monosomy X
Fetal sex
Time
Price
T21
V
X
X
X
V
6 to 9 days
175.00 €
Purchase
Harmony
V
V
V
V
V
3 to 5 days
415.00 €
Purchase

How does it work?

  1. descarga el PDF
    Download the order details from your private area.
  2. descarga el PDF
    Go to an extraction centre.
  3. instrucciones de uso
    One of our partner labs makes the analysis.
  4. instrucciones de uso
    You receive the results.
go further
Why should you request this service?
What is the purpose of this analysis?
  • To detect the presence of the genetic marker causing the Down syndrome in the foetus (chromosome 21 trisomy).
  • To answer your doubts and concerns with a simple blood draw analysis.
  • To know, if you wish, your future baby's gender.
  • To enable you to take preventative measures, always into the current regulations, in case of detection.
Should you do it?
  • If you are older than 35 years.
  • If you present fetal abnormalities.
  • If you previously had a pregnancy with abnormalities in chromosome number.
  • If you present hereditary risk of abnormal chromosome number.
  • If a high risk of abnormal chromosome number was detected by the biochemical screening in the first trimester.
Additional information
¿What is qNIPT technique?
  • qNIPT determines differences between methylation patterns in specific maternal and foetal DNA genetic regions. Certain genetic regions of the maternal DNA are hypometilated while the same regions are hypermetilated in the case of foetal DNA. These specific metilated genetic regions are used as DNA biomarkers for detection of the trisomy 21 on the fetus.
  • qNIPT test for trisomy 21 detection is an reliable and robust method appropiate for clinical routine, according to international medical associations.
q-NIPT T21 by q-PC Test limitations
  • This method is based in the cuantification of allelic dose, so it is restricted to structural anomalies.
  • Since foetal DNA proceed from apoptosis from trophoblast cells, q-NIPT T21 by q-PCR Test can throw false-positive or false-negative results because of placenta confined mosaicism and foetal mosaicism.
  • In case of twin pregnancy with evanescent foetus presence, q-NIPT T21 by q-PCR Test cannot be done.
  • Presence of CNVs (copy number variations).
  • This test is only for singleton gestations.
  • Maternal alterations: alterations that can affect or limit the test results (preeclampsia, heparin treatment, overweight…).
  • The results can be altered by presence of mutations or unclassified variations.

More information

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