Baby Sensor

Many people carry genetic defects that can manifest as hereditary diseases in their children. Unfortunately, these diseases are not immediately recognized in newborns, which can lead to lifelong health impairments that could have been prevented with early intervention.

 

Our Baby Sensor offers a comprehensive examination of urine samples, analyzing over 250 different metabolites. This makes it possible to diagnose more than 100 congenital metabolic disorders early. This analysis is among the most comprehensive methods worldwide for early detection of such conditions.

 

After the examination, parents receive a detailed report explaining not only the results but also potential complications. The Baby Sensor supports health prevention in infants and helps to identify genetic diseases early on, enabling timely preventive or therapeutic measures.