Genomics at the service of future parents
A complete genetic study to support family planning
Prevention starts with pregnancy planning
DNA.files PARENT is a genetic study that analyses if the future parents are carriers of mutations that can be transmitted to their children.
A safe and peaceful pregnancy
Through the DNA.files PARENT it is possible to follow the pregnancy, in cases of infertility and pregnancy losses.
Why DNA.files PARENT?
is the probability of a baby to develop a disease if both parents are carriers of an autosomal recessive disease.
A study designed for future parents
DNA.files PARENT allows the future parents to consider different types of conception, in case they are carriers, in order to prevent the development of serious hereditary diseases.
How does heredity work?
What is a carrier?
A carrier is a person who has a mutation in a gene responsible for causing a recessive disease. The carrier is healthy, that is, does not develop symptoms associated with the respective disease.
And if both parents are carriers?
When both members of the couple carry a mutation associated with an autosomal recessive disease, their children have a 25% chance of having the disease.
Benefits for parents
Preconception genetic study
Screening for mutations in genes associated with severe disease with an autosomal recessive pattern of inheritance.
DNA is obtained from a saliva sample, quickly and painlessly.
Early detection, informed choices
Detection of disease-associated mutations before pregnancy allows parents to consider different conception options.
More than health, we bring tranquility to families
Sequencing of 20 000 genes
Analysis of genetic alterations
Screening for the risk of inherited recessive genetic diseases
Issuance of Clinical Report