Genetics for baby health.
The most comprehensive genetic study to screen diseases in babies and children from a simple saliva sample.
The most comprehensive postnatal genetic service.
As a complement of the current newborn screening programs, this genetic service allows early screening for more than 300 paediatric diseases before the onset of the first symptoms.
A non-invasive analysis for newborns, babies and children.
DNA is collected from a saliva sample in a quick and painless way, without any risk to the child. All screened diseases have a clinical follow-up.
Know to prevent.
- Sequencing of the 20,000 human genes
- Genetic analysis and Clinical report
- Data storage for future clinical usages
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Keep up with the most recent scientific advances on baby healthcare in the era of Genomic Medicine.
