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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.
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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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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.

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+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.
icono de tiempo 3 - 5 days
icono de mundo Spain
icono de la muestra Blood
icono de genes Microarray
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
  • 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
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)
◷ Cita previa WhatsApp 0034 680 260 118, horario lunes-viernes: 9:45 a 12:00
☏ Information: +34 911 284 591
Albacete
Albacete
(Albacete)
◷ Cita previa WhatsApp 0034 680 260 118
☏ Information: +34 911 284 591
Asturias
Gijón
(Asturias)
◷ Cita previa WhatsApp 0034 680 260 118, horario lunes-viernes: 8:00 a 12:00
☏ Information: +34 911 284 591
Oviedo
(Asturias)
◷ Cita previa WhatsApp 0034 680 260 118, horario lunes-viernes: 8:30 a 12:30
☏ Information: +34 911 284 591
Ávila
Ávila
(Ávila)
◷ Cita previa WhatsApp 0034 680 260 118, horario lunes-viernes: 8:00 a 12:45
☏ Information: +34 911 284 591
Badajoz
Zafra
(Badajoz)
◷ Cita previa WhatsApp 0034 680 260 118, horario lunes-viernes: 11:00 a 13:00
☏ Information: +34 911 284 591
Baleares
Palma de Mallorca
(Baleares)
◷ PREVIA PETICION DE CITA
☏ Information: +34 911 284 591
Barcelona
Barcelona
(Barcelona)
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Burgos
Burgos
(Burgos)
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☏ Information: +34 911 284 591
Cáceres
Cáceres
(Cáceres)
◷ Cita previa WhatsApp 0034 680 260 118, horario lunes-viernes: 12:30 a 14:30
☏ Information: +34 911 284 591
Plasencia
(Cáceres)
◷ Previa petición de cita
☏ Information: +34 911 284 591
Cáceres
(Cáceres)
◷ Cita previa WhatsApp 0034 680 260 118, horario lunes-viernes: 11:00 a 12:00
☏ Information: +34 911 284 591
Castellón
Castellón
(Castellón)
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Ciudad Real
Ciudad Real
(Ciudad Real)
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Córdoba
Córdoba
(Córdoba)
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Fuerteventura
Puerto del Rosario
(Fuerteventura)
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Granada
Granada
(Granada)
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La Rioja
Logroño
(La Rioja)
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Calahorra
(La Rioja)
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Lanzarote
Arrecife
(Lanzarote)
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☏ Information: +34 911 284 591
Las Palmas
Las Palmas De Gran Canaria
(Las Palmas)
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León
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Lugo
◷ Previa petición de cita
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Madrid
◷ Previa petición de cita
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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)
◷ Lunes a Viernes de 08.30 a 12.00 horas.
☏ Information: +34 911 284 591
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)
◷ Lunes a Viernes de 08.00 a 11.00 horas.
☏ Information: +34 911 284 591
Madrid
(Madrid)
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☏ Information: +34 911 284 591
Parla
(Madrid)
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Madrid
(Madrid)
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Murcia
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Navarra
Pamplona/Iruña
(Navarra)
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☏ Information: +34 911 284 591
Palencia
Palencia
(Palencia)
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Pontevedra
Pontevedra
(Pontevedra)
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Vigo
(Pontevedra)
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Salamanca
Salamanca
(Salamanca)
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Santander
Santander
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Torrelavega
(Santander)
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Sevilla
Alcalá De Guadaira
(Sevilla)
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Mairena del Aljarafe
(Sevilla)
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Sevilla
(Sevilla)
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Carmona
(Sevilla)
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Sta Cruz De Tenerife
Santa Cruz De Tenerife
(Sta Cruz De Tenerife)
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Toledo
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Toledo
(Toledo)
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Valencia
Mislata
(Valencia)
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☏ Information: +34 911 284 591
Valencia
(Valencia)
◷ Lunes a Viernes de 08.30 a 10.30 horas.
☏ Information: +34 911 284 591
Valencia
(Valencia)
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Gandía
(Valencia)
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Oliva
(Valencia)
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Sagunto
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Valencia
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Valladolid
Valladolid
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Zamora
Zamora
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Zaragoza
Zaragoza
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Zaragoza
(Zaragoza)
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☏ Information: +34 911 284 591

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 €
Harmony
V
V
V
V
V
3 to 5 days
415.00 €

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?
  • 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.

More information

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