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. Prenatal screening 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 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 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. 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 Perinatal genetic screening allows parents to make informed decisions and the specialist to tailor the baby’s medical care from the very beginning. Are you interested in offering myBabyHealth from Veritas? Contact us and find out how we can work together. CONTACT US 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. 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. What is Whole Genome Sequencing (WGS)? Whole genome sequencing is reading the billions of letters in your DNA, a long chain made up of As, Ts, Cs, and Gs. All your genes are encoded with this 4-letter code, so we analyze your sequence and subsequently look for changes or variants in the genes. What is the NGS? NGS comes from the English term, Next Generation Sequencing, and is used to refer to the set of technologies used to sequence millions of DNA fragments in parallel, improving response times and the cost of genetic tests. Before the implementation of NGS sequencing, sequencing a genome cost millions of dollars.riants in the genes. What is DNA? DNA is the genetic blueprint of life. It is a complex molecule that is found within every cell of our body and contains all the necessary instructions to create and maintain life. It is an information storage system, a code written with four letters that represent four molecules: adenine, thymine, guanine and cytosine. The complete sequence of these chemicals makes up our genetic code, our genome. A single DNA molecule contains around 6 billion A’s, T’s, C’s and G’s, in fact, if you could unfold a DNA molecule it would measure almost 2 meters. Why sequence the entire genome? Whole genome sequencing allows all your genetic material to be read by creating a library about you. In this way you will be able to know the relevant information today to prevent and have access to updates in the future, accessing your library again. This trip makes it possible that from now on you can personalize, with the help of your specialist, your health care based on what makes you unique: your DNA. What does it mean to have a genetic variant? All people have thousands of genetic variants in their DNA, but it doesn’t mean that they will develop a genetic disease. There are variants that simply make us unique, others that slightly increase our probability of developing a disease, and others that require medical attention because they pose a risk to our health. Interpretation of genetic reports should always be done during a consultation with a genetic counselor to help you understand the information. Is it bad to be a carrier of a genetic mutation? Each person can present alterations and variations in their DNA that give them characteristics that make them unique. Detecting these variations is a benefit since it will help to establish guidelines and opportune measures to reduce the possibility of developing the disease and / or treat it in an anticipated and more effective way. Will I suffer from a certain disease because I am a carrier of a disease of genetic origin? No, being a carrier of a genetic disease is common. Humans have two copies of each gene. Being a carrier means that you have a genetic variant in one of the copies of a gene associated with a recessive disease. In other words, it has one copy of the gene that works and one copy that does not work. Recessive diseases require that an individual have two variants (the two copies of the gene that do not work) to develop the disease, therefore, you are a “carrier” of a variant, but are not at risk of developing this disease. However, knowing this information is very important since you are at risk of having children affected by this disease if your reproductive partner is also a carrier of the same pathology. Can my genome change over time? No. The genetic information of a person does not change, what advances is scientific knowledge for which fortunately we know more every day. For this reason, the genome is a resource for life and that can be consulted over time to find out new findings that have been produced thanks to the advancement of scientific knowledge. Why does pricing for genetic tests vary so much? The cost of a genetic testing service is related to the technology utilized and the amount genetic expertise is required to provide the result. There is a direct correlation between the amount of DNA information analyzed and the more clinically impactful and reliable the result will be. At Veritas we use whole genome sequencing that allows for the capture and analyzing of all of a person’s DNA. Because the information is so valuable and can significantly impact a person’s future healthcare, we believe it should be managed by a medical professional. We support either directly or in collaboration with the prescribing physician the pre and post-test genetic counseling process where the results are explained and an action plan is established to fully benefit from the information provided. What are chromosomes? DNA is not dispersed in our cells, it is carefully packed into structures called chromosomes. We have 46 chromosomes in total, half inherited from our mother and half from our father. Located on these chromosomes are segments of DNA called genes, many of them contain instructions for making proteins, and it is these proteins that determine everything about us, from the color of our eyes to our susceptibility to disease.