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Addressing the Limitations of Newborn Screening Programs. The statistic is jaw-dropping – 70% of genetic rare diseases start in childhood. While newborn screening has evolved into an effective public health program to enable early intervention for many conditions, unfortunately there are many treatable rare genetic disorders that current newborn screening programs do not test for, resulting in devastating outcomes for many individuals and their families afflicted by these disorders. At Key Proteo, we envision a world in which early intervention through early, enhanced detection is available for every child, everywhere. With our novel proteomics-based platform, we aim to improve early screening programs, with the goal that every newborn is screened for a wider range of treatable conditions. By focusing on these critical unmet needs, we are working to drive better outcomes for future generations. Join us on this journey, because no treatable genetic disorder should go unseen. Learn more at: Key Proteo: www.keyproteo.com #APHL #AssociationofPublicHealthLaboratories #PublicHealth #APHLNBS #NewbornScreening #KeyProteo #Proteomics #WilsonDisease #WilsonDiseaseAssociation #WiskottAldrichSyndrome #XLA #AdenosineDeaminaseDeficiency

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