Significance of Newborn screening
Newborn screening is a public health initiative that tests infants shortly after birth for various genetic conditions. It aims to identify disorders such as Duchenne muscular dystrophy, Pompe disease, and sickle cell disease through blood tests. This early detection enables timely intervention and management, improving health outcomes for affected infants. By implementing this program, healthcare providers can ensure that necessary treatments begin as soon as possible, emphasizing the importance of newborn screening in pediatric care.
Synonyms: Neonatal screening, Early screening
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The concept of Newborn screening in scientific sources
Newborn screening is a public health initiative that tests newborns for genetic disorders like Pompe disease, facilitating early diagnosis and treatment, ultimately enhancing health outcomes for affected infants.
From: The Malaysian Journal of Medical Sciences
(1) This is a public health program designed to identify certain health conditions in newborn babies, and is utilized for the detection of severe combined immunodeficiency and T-cell lymphopenia, and is an important aspect of preventative medicine.[1] (2) A program designed for the early diagnosis and preventive treatment of life-long impairments in infants, recommended by the World Health Organization for the primary prevention of congenital anomalies.[2]