myBabyHealth myBabyHealth Perinatal genetic screening service myBabyHealth myBabyHealth combines the non-invasive prenatal test myPrenatal and the myNewborn neonatal genetic screening test, in order to perform the most complete genetic screening before and after the birth of the baby. myBabyHealth is the most complete service for parents-to-be with the best conditions. myBabyHealth includes: Prenatal screening – myPrenatal This is an advanced prenatal screening test or non-invasive prenatal test that is performed from the week 10 of pregnancy and studies the most common chromosomal abnormalities: Down, Edwards and Patau syndromes (trisomies 21, 18 and 13), together with alterations in the sex chromosomes. Veritas also offers myPrenatal GenomeScreen, which allows the study to be extended to a more complete screening. READ MORE ABOUT MYPRENATAL Postnatal screening – myNewborn Genetic screening test to personalise the newborn’s medical care from day one by analysing more than 400 genes related to 390 diseases that can affect the newborn in the early stages of life, allowing to adapt their medical care. myNewborn is indicated in any newborn or child without symptoms of genetic disease, as part of their medical care. READ MORE ABOUT MYNEWBORN Are you interested in offering myBabyHealth from Veritas? Contact us and find out how we can work together. CONTACT US Are you interested in myBabyHealth 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. FIND OUT MORE PATIENT BROCHURE Advantages of myBabyHealth myBabyHealth provides the most comprehensive health screening of the baby-to-be before and after birth. Both tests are performed without risk to the mother or the baby-to-be. myBabyHealth has been developed by the Veritas medical team, experts in DNA sequencing and analysis with the most advanced technology. The service offers preferential conditions for parents who request this pack. We have a team of experts with more than 20 years of experience in prenatal diagnosis and genetic counselling. “Perinatal genetic screening allows parents to make informed decisions and the specialist to tailor the baby’s medical care from the very beginning.” 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 myBabyHealth you can contact us. Recurso 27CONTACT Frequently asked questions about myBabyHealth How does the myBabyHealth test work?myBabyHealth is a perinatal service that combines a prenatal screening (myPrenatal) with a neonatal one (myBabyHealth), which, when packaged, are obtained under conditions that are especially advantageous for parents. Prenatal screening, our myPrenatal NIPT, is performed with a simple blood sample (like any routine analysis) from which free fetal DNA is extracted, and can be performed from the 10th week of gestation. For its part, myNewborn neonatal screening is carried out with a sample of the baby's saliva, and can be carried out from the moment of birth. When should myBabyHealth be done?Each test has its own indications, the myPrenatal non-invasive prenatal test is indicated for any pregnant woman of legal age from the 10th week of gestation. myNewborn can be done from the moment of birth. SEE ALL QUESTIONS
