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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.
Week 10
From the tenth week of gestation
99'9%
The analysis is almost 100% reliable(1)
so you can trust that the result will be accurate.
0 risk
Non-invasive analysis
It only requires a blood sample and has no danger to the baby.
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.
+50
We have more than 50 collaborating centers
where to perform the blood draw without an appointment.
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.
- A genetic advisor referenced by medmesafe will contact you and explain the results.
6 - 9 days
Spain
Blood
Next Generation Sequencing - Business days from receipt of the sample in the Laboratory
- Only available in Spain at the moment
- Sample of blood
- 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).
* Up to 10% cheaper than lab fee and including explanation of results by a genetic counselor
Access the most extensive and reputable laboratory network
⌖ More than 50 centers in Spain
○ To perform the extraction, it is not necessary to go on an empty stomach
○ To perform the extraction, it is not necessary to go on an empty stomach
A Coruña
Albacete
Asturias
Avilés
(Asturias)
(Asturias)
◷ Lunes a Viernes de 08.00 a 21.30 H. Sábados y Domingos de 9.00 a 21.00 H.
☏ Information: +34 911 284 591
Gijón
(Asturias)
(Asturias)
◷ Lunes a Viernes de 08.00 a 14.00 horas. Tardes de 17.00 a 19.00 horas.
☏ Information: +34 911 284 591
Ávila
Badajoz
Badajoz
(Badajoz)
(Badajoz)
◷ Lunes a Viernes de 08.00 a 12.00 horas. Sábados de 09.00 a 11.00 horas.
☏ Information: +34 911 284 591
Barcelona
Burgos
Cáceres
Cáceres
(Cáceres)
(Cáceres)
◷ Lunes a Jueves de 08.00 a 14.00 horas. Tardes de 16.00 a 20.00 horas. Viernes de 08.00 a 14.00 horas.
☏ Information: +34 911 284 591
Córdoba
Córdoba
(Córdoba)
(Córdoba)
◷ Lunes a Viernes de 08.00 a 12.00 horas. Tardes de 16.00 a 18.30 horas.
☏ Information: +34 911 284 591
Granada
Huelva
La Rioja
Logroño
(La Rioja)
(La Rioja)
◷ Lunes a Viernes de 08.00 a 13.00 horas. Tardes de 17.00 a 19.00 horas.
☏ Information: +34 911 284 591
Las Palmas
Las Palmas De Gran Canaria
(Las Palmas)
(Las Palmas)
◷ Lunes a Viernes de 07:00 a 11:30 horas. Sábados de 9 a 11 H.
☏ Information: +34 911 284 591
León
León
(León)
(León)
◷ Lunes a Viernes de 08.00 a 14.00 horas. Tardes de 17.00 a 18.30 horas. Sábados previa cita.
☏ Information: +34 911 284 591
Lugo
Madrid
Madrid
(Madrid)
(Madrid)
◷ Lunes a Viernes de 08.00 a 18.30 horas. Sábados de 08.30 a 10.30 horas.
☏ Information: +34 911 284 591
Madrid
(Madrid)
(Madrid)
◷ Lunes a Viernes de 08.00 a 18.30 horas. Sábados de 08.30 a 10.30 horas.
☏ Information: +34 911 284 591
Parla
(Madrid)
(Madrid)
◷ Lunes a viernes de 11:00 a 12:00 h. Previa cita. Sábados de 9:30 a 11:30 h. Sin cita previa.
☏ Information: +34 911 284 591
Murcia
Navarra
Pamplona/Iruña
(Navarra)
(Navarra)
◷ Lunes a Viernes de 08.00 a 15.00 horas. Tardes de 16.00 a 18.00 horas.
☏ Information: +34 911 284 591
Palencia
Pontevedra
Santander
Santander
(Santander)
(Santander)
◷ Lunes a Viernes de 08.00 a 18.30 horas. Sábados de 09.00 a 11.00 horas.
☏ Information: +34 911 284 591
Sevilla
Alcalá De Guadaira
(Sevilla)
(Sevilla)
◷ Lunes a Viernes de 08.30 a 13.30 horas.
☏ Information: +34 911 284 591
Mairena Aljarafe
(Sevilla)
(Sevilla)
◷ Lunes, Miércoles y Viernes de 9.00 a 13.00
☏ Information: +34 911 284 591
Sevilla
(Sevilla)
(Sevilla)
◷ Lunes a Viernes de 8.30 a 13.30; Miércoles y Jueves de 16.00 a19.00
☏ Information: +34 911 284 591
Sevilla
(Sevilla)
(Sevilla)
◷ Lunes a Viernes de 08.00 a 13.00 horas. Tardes de 17.00 a 20.00 horas (excepto los Miércoles)
☏ Information: +34 911 284 591
Sta Cruz De Tenerife
La Laguna
(Sta Cruz De Tenerife)
(Sta Cruz De Tenerife)
◷ Lunes a Viernes de 08.00 a 10.00 horas.
☏ Information: +34 911 284 591
Santa Cruz De Tenerife
(Sta Cruz De Tenerife)
(Sta Cruz De Tenerife)
◷ Lunes a Viernes de 07.00 a 17.00 horas. Sábados de 08.00 a 10.00 horas.
☏ Information: +34 911 284 591
Toledo
Toledo
(Toledo)
(Toledo)
◷ Lunes a Viernes de 08.00 a 14.00 horas. Tardes de 16.30 a 18.30 horas. Sábados previa cita.
☏ Information: +34 911 284 591
Valencia
Mislata
(Valencia)
(Valencia)
◷ Lunes a Viernes de 08.00 a 20.00 horas. Sábados de 09.00 a 13.00 horas.
☏ Information: +34 911 284 591
Valladolid
Valladolid
(Valladolid)
(Valladolid)
◷ Lunes a Viernes de 8.00 a 18.00 H. Sábados de 8.00 a 11.00 H.
☏ Information: +34 911 284 591
Zamora
Zaragoza
Salamanca
How does it work?
-
Download the order details from your private area. -
Go to an extraction centre. -
One of our partner labs makes the analysis. -
Your healthcare professional presents your results.
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.