Down syndrome (Trisomy 21 test)

Non-Invasive test (results availables in 6-9 days)

	Detection of Down syndrome (trisomy 21) and the option of knowing the gender of the future baby if you wish.
	The test is performed through a maternal blood sample, so it does not represent any risk to the fetus or the mother.
	Official results available in 6-9 business days since obtaining the sample in the laboratory (CE-IVD certificate).
	You can go to any of our more than 150 associated centers without having to fast. Open from Monday to Friday, (to know the opening hours of each center, please click below and select the city).
	Receive a genetic counseling appointment for the explanation of your results, at no additional cost. (This service is optional).

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Information:

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).

We put at your disposal more than 150 extraction points, the largest network in Spain.

It allows you to detect the presence of genetic markers in the fetus of Down syndromes at an early stage of pregnancy.
You can avoid invasive tests like amniocentesis, which are uncomfortable and dangerous for both, mother and baby.
Allows you to take decisions based on the current legislation.

It will give you peace of mind about your pregnancy from week 10, superior accuracy (less than 0.1% false positives).
If you had previous pregnancies with the presence of trisomies.
If it is your first pregnancy and you are over 35 years old.
If you have fetal ultrasound abnormalities.
If you have a high hereditary risk of fetal aneuploidies.

The Non-invasive Prenatal Test is a maternal blood test that detects the main chromosomal alterations of the baby, avoiding the possible risks of amniocentesis.
When you are pregnant, your blood contains fragments of your child's DNA. This test has greater accuracy and a lower rate of false positives; compared to traditional invasive tests.

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.
It is a highly precise quantification technique with a sensitivity and specificity greater than 99%.
The test is validated for use in single and twin pregnancies and IVF (own egg or egg donation).

Go Up

	T21	Harmony
Trisomy 21 - (Down's syndrome) :
Trisomy 18 - (Edward’s syndrome) :	X
Trisomy 13 - (Pateu’s syndrome) :	X
Monosomy X - (Turner’s syndrome) :	X
Fetal sex :
Time of results :	6 to 9 days	3 to 5 days
Price in center :	~~199,00 €~~	~~485,00 €~~
Exclusive price on this website:	175,00 €	349,00 €
	Purchase	Purchase