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Non Invasive Prenatal Test

Detects Down syndrome, Edwards syndrome, Patau syndrome, Turner syndrome, and even the future sex of the baby from week 10.

	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.
	The test is performed through a maternal blood sample, so it does not represent any risk to the fetus or the mother.
	Results available in 6 business days since obtaining the sample in the laboratory. Official results.
	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:

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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, Edwards, and Patau syndromes at an early stage of pregnancy.
You can avoid invasive tests like amniocentesis, which are uncomfortable for both mother and baby.
Allows you to take decisions based on the current legislation.

It will provides you peace of mind about your pregnancy 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.

The prenatal test analyzes fragments of specific chromosomes using microarray technology.
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).

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Below you can see what each test modality analyzes, and below this table more details

	Prenatal Test	Prenatal Test Plus
Trisomy 13:
Trisomy 18:
Trisomy 21:
Aneuplodias:	X
Microsensing:	X
Deletions:	X
Fetal gender:
Time of results (business days):	6	6
Genetic consultation:
Price at center €:	~~495,00~~	~~720,00~~
Medmesafe price €:	460,00	590,00
Choose your test >>	Purchase	Purchase