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Diagnostics in Newborns

FGF has the powerful ability to identify the genetic defects responsible for various diseases, and thereby its utilization can reveal genetic markers for particular diseases.

The availability of molecular/genetic markers (mutations) associated with particular disease phenotypes aids in the identification of the potential for any given disease in newborns.

  • Helps predict future disease potential in newborns
  • Early identification enables children to receive early treatment, such as lifestyle changes and other medical measures
  • Facilitates personalization of medicine
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