Always focusing on tailoring the approach for each patient.
Tomorrows’ Reproductive Medicine
This is our way to name the new frontiers reached over the last decade in the field of reproductive genomics, thanks to the advancements in next generation sequencing (NGS).
Next Generation Sequencing (NGS)
Allowing us to stratify patients according their reproductive phenotypes, pharmacogenomics (PGx) and molecular embryology, widening our knowledge to improve treatments against infertility and reproductive health, adopting a proactive approach by understanding the molecular and genetic basis of reproductive processes.
Did you know that around 10 to 15% of all couples in reproductive ages (20 to 45 years old) are infertile?
Infertility can be due to a series of factors and a major component to it comes from habits and environment. Still there are physiological, genetic and molecular aspects to it, that may be the cause of why you and your partner haven’t achieved the pregnancy you both so long desire.
The important thing to know is that 1 out of 3 cases of infertility are due to a combination of both male and female factors and that it is NO ONE’s fault.
Such factors encompass hormonal levels, metabolism, ovulation, sperm production, sexual organs structural variations, STDs, exposure to chemical substances and physical phenomenon, to mention a few.
Early genomic family planning
Starting a family is a great couple’s decision, which includes a lot of thinking, concerns and joy. Nevertheless, there is TODAY a critical step within genetic health to be considered, before deciding to get pregnant.
Did you know that is estimated that ALL of US have at least 3 genetic variants of high risk (pathogenic) that could be passed down to our children?
When fecundation happens and the parents’ genetic material recombines, when a gene or set of genes are affected in both, confers a very high chance that such baby is born with a genetic disease, which most of them are serious and lethal, to the extent that most kids affected with them don’t survive past their 5th birthday.
Extended Carrier Screening Test
Theranomics offers you our extended carrier screening test that will allow for you and your partner to rule out wether or not you share a mutation that could affect the health of the baby you’re already planning to have. By taking our test you could reduce up to 90% of the risk associated to diseases caused by one gene, providing you with the certainty you need for the wonders of parenthood and the joy of a planned pregnancy.
Pregnancy is an unparalleled experience for expecting paretns and we know that you’ve been constantly following up with medical appointments, taking care of your diet, sleep and schedules to have a carefree experience.
Nevertheless, the procedure to obtain such samples (biopsy) could induce a miscarriage (1% of all cases) even when the karyotype would have resulted normal.
That’s why you need our TheraNIPS test to remain sure that your pregnancy maintains its course.
7 years of experience and pioneers within the industry
We have helped over 1290 families to find a diagnosis and treatment, thanks to our theranostic approach.