The document provides an overview of the newborn screening program at the Kuwait Medical Genetic Center, emphasizing its critical role in early detection of rare health conditions to ensure better health outcomes for infants. It includes detailed annual statistics, screening results, and the expansion of the disease panel from 2014 to 2017, which composed of disorders such as phenylketonuria and congenital hypothyroidism. Furthermore, it highlights sample collection data, gender and nationality distributions, and positive predictive values for various conditions screened in the program.