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Non-invasive prenatal test harmony
Detects Down, Edwards and Patau syndromes, sexual aneuploidies 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 chromosomal abnormalities 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.
3 - 5 days
Harmony 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 harmony
- Detection of Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), Patau syndrome (trisomy 13) and Turner syndrome (Monosomy X)
- 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.
3 - 5 days
Spain
Blood
Microarray - Business days from receipt of the sample in the Laboratory
- Only available in Spain at the moment
- Sample of blood drawn at an extraction center.
- Analyze fragments of specific chromosomes using microarray technology.
- It is a highly accurate quantification technique with a sensitivity and specificity greater than 99%.
- The Harmony is validated for use in single, twin and IVF pregnancies (own ovum or ovodonation).
- Indicated for pregnant women of advanced age (+35 years).
- In the case of pregnancies of two fetuses or twin, only chromosomes 21, 18 and 13 will be analyzed (Sexual aneuploidies will not be detected and fetal sex will be reported as long as one of the babies is a child, or the two babies be girls).
- What is a non-invasive prenatal test (NIPT) ?:
- When you are pregnant, your blood contains fragments of your child's DNA.
- this test analyzes this DNA in your own blood avoiding any impact on the fetus itself and has a higher accuracy and lower false positive rate than traditional invasive tests such as amniocentesis
* Up to 10% cheaper than lab fee
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
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
Baleares
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
Castellón
Ciudad Real
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
Fuerteventura
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
Lanzarote
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
Salamanca
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
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
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
Vizcaya
Zamora
Zaragoza
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. -
You receive the results.
Why should you request this service?
What is the purpose of this analysis?
- For evaluating the fetal risk of having trisomies 21, 13 and 18.
- Optional analysis of fetal sex.
- To resolve your doubts and concerns with a simple blood analysis.
- To allow you to apply preventive measures, within existing legislation, in case of detection.
Should you do it?
- If you would like a precision analysis that when used in more than one million pregnancies from early gestational stages (tenth week), had a less than a 0.1% false-positive rate when contrasted with blinded studies.
- If you are an over 35 year old gestant.
- If fetal anomalies were detected on an ultrasound scan.
- If you had a previous gestation presenting aneuploidy (fetal chromosome number change).
- If you present hereditary fetal aneuploidy risk.
- If a high aneuploidy risk was detected at the first quarter biochemical screening.
Additional information
What is a prenatal non-invasive test?
- When you are pregnant, your blood contains fragments of your child's DNA.
- This test analyzes fetal DNA in your blood avoiding any impact on the fetus, presenting more precision, and a lower false-positive percentage than traditional invasive tests like amniocentesis.
What technologies applies?
- The Harmony test analyzes fragments of specific chromosomes using the 'microarray' technology.
- It's an extremely precise quantification technique with a sensitivity and specificity higher than 99%.
- The Harmony test is validated to use in unique pregnancies, twin pregnancies, and egg donation pregnancies.