Thanks to the latest progress in the field of Genomics and Next Generation DNA Sequencing technologies (NGS), genetic testsallows mosteffective preventive actions for the whole family.
Understanding each patient genetic profile by performing genetic testing individualizes the approach to disease prevention, detection, diagnosis, treatment and management.
Jouvene has selected the best Prenatal Genetic Diagnostics with an optimally automatized workflow to certify consistency and reproducibility of results. Our unique expertise, ensures that the BioInformatics infrastructures are designed with Confidential Patient Information and Data Security in mind, confirming our track record in personal data handling.
Non Invasive Prenatal Testing (NIPT) is a method of determining the risk that the fetus could be born with certain genetic abnormalities. Chromosomal disorders are caused by the presence of an extra or missing copy (aneuploidy) of a chromosome.
NIPT primarily screens for Down syndrome(trisomy 21, caused by an extra chromosome 21), trisomy 18 (caused by an extra chromosome 18), trisomy 13 (caused by an extra chromosome 13), and extra or missing copies of the X chromosome and Y chromosome (the sex chromosomes). The test may also include screening for additional chromosomal disorders that are caused by missing (deleted) or copied (duplicated) sections of a chromosome.
We are a passionate and truly committed team with a clear mission to help people have a better knowledge about their health and the one of their family, by providing simple, reliable and affordable services. Jouvene invests families and doctors with information at the right timing leading to appropriate medical decisions.