Non-invasive prenatal test harmony
Detects Down, Edwards and Patau syndromes, sexual aneuploidies and fetal sex from the 10th week of pregnancy
so you can trust that the result will be accurate.
It only requires a blood sample and has no danger to the baby.
which offers the answers you are looking for in a few days for your tranquility and relaxation.
where to perform the blood draw without an appointment.
- 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.

- 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

○ 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)
(Asturias)
(Asturias)
(Ávila)
(Badajoz)
(Cáceres)
(Cáceres)
(Madrid)
(Madrid)
(Madrid)
(Sta Cruz De Tenerife)
(Valencia)
How does it work?
-
Download the order details from your private area.
-
Go to an extraction centre.
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One of our partner labs makes the analysis.
-
You receive the results.
- 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.
- 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.
- 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.
- 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.