Non-invasive prenatal test
- DETECTS chromosomal abnormalities in the fetus from week 10 of pregnancy with a reliability of over 99%.
- Completely and safely analyzes all chromosomes as well as the presence of duplications and deletions.
- KNOW the results in just 3 days with a test conducted entirely in Spain.
Non-invasive prenatal test
625,00 €
Especially recommended in the following cases:
- Pregnant women over 35 years of age.
- Pregnant women with a high risk of presenting fetal chromosomal abnormalities according to the triple screening or combined screening of the first trimester.
- Pregnant women with previous pregnancies affected by a chromosomal abnormality or previous repeated miscarriages without a known cause.
- Pregnant women with ultrasound markers indicating the presence of a chromosomal abnormality.
- To pregnant women or couples with an altered karyotype.
RESULTS
To take care of your baby from day one
What results can I get from the prenatal test?
- Low risk : This means that the DNA levels are comparable to a normal chromosome set and that, therefore, it is very unlikely that the baby will have any of the abnormalities analyzed.
- High risk : This means there is a high probability that the baby has the syndrome or disorder being tested. If the result is positive, the test includes confirmation of the results through amniocentesis or chorionic villus sampling.
Do you have any questions?
We recommend you request a free initial visit so our doctors can learn about your case and answer any questions you may have.
Step by step
How does it work?
Sample extraction in one of our centers
After purchasing the prenatal test, we will schedule an appointment at your nearest center (see our network of centers here ), and we will provide you with the document you must bring to the appointment.
Sample analysis and results in 3 days
Your results will be available by email within 72 business hours of receiving your sample at the laboratory.
Visit to explain results
After receiving the report, you can request the results explanation visit included in the test. This visit is conducted online with one of our doctors.
Visit with the specialist included
· Advice
· Interpretation of results
Object of study
What diseases or syndromes are included?
The test analyzes all 24 chromosomes, identifies the baby’s sex, and detects deletions and duplications with a resolution similar to that of a karyotype.
- Trisomy of chromosome 21
- Trisomy of chromosome 18
Trisomy of chromosome 13
- Turner syndrome (45, X)
- Klinefelter syndrome (XXY)
- XYY syndrome
- Trisomy X
Sex chromosome analysis not valid in twin pregnancies.
Analysis of any chromosomal abnormalities in the remaining chromosomes
Detection of any deletion or duplication larger than 7 Mb
— Our Commitment
Rigor, quality, and technology
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We only analyze variants with solid scientific evidence
Our expert panel selects and reviews variants with solid scientific evidence based on scientific literature and medical guidelines.
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Quality Assurance
The laboratory where samples are processed and analyzed holds ISO 15189 and 9001 certifications.
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We use the best technology available
We use the PMDA (Precision Medicine Diversity Array) platform by Applied BioSystems, which enables the analysis of over 850,000 genetic markers in your DNA with a quality rate over 99%. It is the most comprehensive platform on the market, designed to cover all relevant genetic variants related to your health. This platform includes genetic variants from all ancestral populations and also provides analysis of specific mitochondrial DNA and Y chromosome markers, allowing for a deeper and more accurate understanding of your ancestral origins.
FAQS
Do you have questions about the prenatal test?
Other people have asked this:
Can a professional explain the results of my study to me?
We recommend discussing the results of your tests with a healthcare professional. You can discuss them with your doctor, nutritionist, or geneticist. If you need expert advice, our professionals are available to provide you with virtual visits lasting approximately one hour to learn about and evaluate your case, propose action and follow-up guidelines, answer any questions, and more.
How do I request visits with a professional?
First of all, you must have booked the service through our online store, either at the time of purchasing the genetic test or later. Once booked, you must schedule your appointment in our online appointment book. Once booked, you will receive an email with the link to the online appointment, so you can access the appointment on the reserved day and time.
— Do you have any more questions?
Ask us your questions
Call us at +34 93 115 99 50, send us a message on WhatsApp, or fill out the form below: