Prenatal diagnostic test - possible genetic alteration

myPrenatalWES

One test, all the power of genetic diagnostics (deletions/duplications and molecular testing)

myPrenatalWES is an innovative prenatal diagnostic test indicated in pregnancies with ultrasound findings with suspected genetic alteration. It consists of sequencing the fetal exome from amniocentesis or chorionic villus sampling for the study of CNVs and other genetic alterations.

The test is especially indicated in:

Diagnostic service aimed at pregnant women in the following situations:

Enlarged nuchal fold, after ruling out aneuploidy

Cardiac malformation

Short femur

IUGR, after ruling out aneuploidy

myPrenatalWES includes:

Veritas offers in a single test a complete prenatal diagnostic service, based on fetal exome sequencing, which includes both Copy Number Variants (CNVs) and targeted analysis of single nucleotide variants (SNVs) based on diagnostic suspicion.

Are you interesting in offering myPrenatalWES from Veritas?

Are you interested in one of our genetic tests but you do not have a doctor that provides the service?

Our medical professionals can help you. Please click on the below button to learn more.

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Advantages of myPrenatalWES

myPrenatalWES brings advantages at different levels:

From a single invasive procedure and single sample it is possible to perform CNVs analysis and molecular studies.

The turnaround time is shortened as the foetal exome sequencing is performed and if a subsequent molecular analysis is needed, only the data analysis is necessary.

In foetuses with a normal result, it is possible to order neonatal screening tests after birth, obtaining a much faster result (myNewborn).

The information obtained from a single sample is maximised.

Advice to the specialist

Veritas offers a differential service by providing advice to the specialist for the interpretation of your patient’s results, whenever you need it.

Are you a medical professional?

If you want more technical information about myPrenatalWES you can download the medical brochure

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Frequently asked questions about myPrenatalWES?

How does myPrenatalWES work?

myPrenatalWES consists of sequencing the fetal exome from amniocentesis or chorionic villus sampling for the study of CNVs and other genetic alterations.

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