PrenatalWES PrenatalWES One test, all the power of genetic diagnostics (deletions/duplications and molecular testing) PrenatalWES 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 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.Advantages PrenatalWES 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. Are you interested in PrenatalWES but you do not have a doctor that provides the service? Our medical professionals can help you. Contact us. FIND OUT MORE Advice to the specialistVeritas 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 PrenatalWES you can download it here DOWNLOAD
