Genomics at the service of your baby

A complete genetic study designed for you baby health
DNA.files BABY

The most complete postnatal service

DNA.files BABY is a genetic study that allows tracking more than 200 paediatric diseases through a simple saliva sample.

Why DNA.files BABY?

1 out of 10

children have a mutation responsible for causing a disease.

70%

of rare diseases have a genetic origin and have a childhood onset.

5 years

to reach a conclusive diagnosis in a case of a rare disease.

7 physicians

are consulted by a patient until reaching a diagnosis.

A study for newborns, infants and children

DNA is obtained through a saliva sample, painlessly, non-invasively and without any risk to the baby.

Benefits for your baby

In Portugal, the Guthrie Test tracks 26 diseases. DNA.files BABY screens for more than 200 pathologies.

Complement to the Foot Test

In Portugal, the Guthrie Test tracks 26 diseases. DNA.files BABY screens for more than 200 pathologies.
All screened diseases have clinical follow-up, that is, their risk can be prevented or mitigated.

Actionable pediatric diseases

All screened diseases have clinical follow-up, that is, their risk can be prevented or mitigated.
The earlier mutations are detected, the faster and more efficient clinical intervention will be.

Early detection, accelerated actions

The earlier mutations are detected, the faster and more efficient clinical intervention will be.

More than health, we bring tranquility to families

Sequencing of 20 000 genes
Analysis of more than 350 genes
Screening for over 200 paediatric diseases
Issuance of Clinical Report
Genetic Counselling
Genetic data storage

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