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Cariochip: Advanced Genetic Analysis for Chromosomal Alteration Identification

Are you looking for answers about possible chromosomal alterations? Cariochip is a high-resolution clinical analysis test that allows the study of the human genome to identify chromosomal abnormalities associated with congenital malformations or developmental and intellectual disorders, both in the prenatal and postnatal stages.

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¿Where is it done?

To purchase this test, fill out the form and we will send you a quote.
If you prefer, you can go directly to a Laboratorio Echevarne center where they will provide you with the necessary information to carry out the test.

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Description

Sometimes, conventional genetic tests do not detect small chromosomal abnormalities that can have a significant impact on health. Cariochip uses state-of-the-art microarray technology (750K resolution), far superior to the 60K of other techniques, to analyze the entire genome and detect more than 250 genetic syndromes that could go unnoticed with traditional methods.

Cariochip Prenatal
Recommended in prenatal studies in cases such as:
Maternal age over 35 years
Abnormal ultrasound findings
History of recurrent miscarriages
Alterations in previous pregnancies
High risk index in triple screening
Abnormal fetal karyotype

Cariochip Postnatal
Indicated in pediatric studies when there are:
Dysmorphic features or congenital malformations
Developmental delay or autism spectrum disorders with normal karyotype
Abnormal karyotype requiring detailed molecular study (duplications, balanced translocations with clinical manifestation)
Cariochip is an essential diagnostic tool to obtain an accurate diagnosis and make informed medical decisions from the earliest stages of life.

Sample type: Prenatal - Amniotic fluid or chorionic villus Postnatal - Blood

Results in days

¿Is it suitable for me?

This test is for you if:
• (Prenatal) You have advanced maternal age, abnormal findings in ultrasounds, or recurrent miscarriages.
• (Postnatal) Dysmorphic features, developmental delay, or autism are suspected.
• Your gynecologist, pediatrician, or clinical geneticist considers this test useful for your case.

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Cariochip: Advanced Genetic Analysis for Chromosomal Alteration Identification

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Benefits

• Detects alterations that go unnoticed in conventional karyotyping.
• Identifies more than 250 genetic syndromes.
• Provides a high-resolution diagnosis for prenatal and postnatal cases.

Results

Your results, clear and accessible:
Within 6 business days, we will send you an SMS.
With that notification, you will be able to access and download your results from our online Patient Portal.
Once you have your report, consult a healthcare professional so they can interpret it with you and, if necessary, create a personalized action plan.

Do I need genetic counseling?

Yes. A genetics specialist will help you understand the findings and decide what steps to take.

Frequently Asked Questions

Does the Cariochip replace the Non-Invasive Prenatal Test (NIPT)?

No. The TPNI is a screening test in maternal blood. The Cariochip is a more detailed diagnostic study that requires a fetal sample or blood in the pediatric case. They are complementary tests.

Can it be done at any time during pregnancy?

It is performed when the doctor indicates obtaining a fetal sample through amniocentesis or chorionic biopsy. It cannot be done with maternal blood alone.

What is the difference between a Cariochip and a conventional karyotype?

The karyotype detects large alterations in the chromosomes. The Cariochip also identifies small changes (microdeletions and duplications) that can have a significant impact on health.

What happens if the result is inconclusive?

Some variants may not be clearly related to a disease. In such cases, follow-up is recommended and, sometimes, family studies to clarify their significance.

Do I need genetic counseling?

Yes. A genetics specialist will help you understand the findings and decide what steps to take.

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Customer Reviews

“

The Cariochip gave us clarity when everything was confusing. Having such a precise result helped us better understand our son's situation and breathe a little easier.

”
Sabadell, Barcelona
“

I decided to do the Cariochip during pregnancy and it gave me peace of mind. It was a clear and detailed report that clarified my doubts.

”
Valladolid

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