Significance of Neonatal screening program
The neonatal screening program is a critical public health initiative focused on the early detection of genetic disorders in newborns. This includes conditions such as hemoglobinopathies and spinal muscular atrophy (SMA). The program employs genetic testing to identify disorders like sickle cell disease, enabling timely interventions and management. By identifying these conditions early, the neonatal screening program aims to improve health outcomes for affected newborns through appropriate and prompt treatment strategies.
Synonyms: Newborn screening program, Newborn screening
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The concept of Neonatal screening program in scientific sources
The Neonatal screening program focuses on the early detection of conditions such as sickle cell disease and spinal muscular atrophy (SMA) in newborns, enabling timely intervention and effective management of these health issues.
From: The Malaysian Journal of Medical Sciences
(1) Health initiatives aimed at early detection of genetic disorders, including hemoglobinopathies, in newborns.[1]