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Newborn screening has been identified as one of the most effective means of disease prevention in the United States by testing every newborn baby for potentially fatal conditions that may not be immediately obvious. By testing babies before symptoms begin, newborn screening programs help prevent disabilities and decrease the newborn mortality rate.
Each year in Tennessee, about 385 babies are born with a rare disorder found with required newborn screening. Across the U.S., rare diseases account for 35% of deaths in the first year of life.
The following disorders are additional conditions that may be detected by screening. Many are listed as "secondary targets" by the 2005 ACMG report. [1] Some states are now screening for more than 50 congenital conditions. Many of these are rare and unfamiliar to pediatricians and other primary health care professionals. [1] Blood cell disorders
Newborn screening programs initially used screening criteria based largely on criteria established by JMG Wilson and F. Jungner in 1968. [6] Although not specifically about newborn population screening programs, their publication, Principles and practice of screening for disease proposed ten criteria that screening programs should meet before being used as a public health measure.
The Newborn Screening Saves Lives Reauthorization Act of 2014 would amend the Public Health Service Act to extend and revise a grant program for screening, counseling, and other services related to heritable disorders. The bill would expand eligible grantees to include a health professional organization and an early childhood health system.
More Middle Tennessee children, from birth to age 5, are receiving early diagnosis and treatment for a wide range of mental health conditions based on federal grant funding from the U.S ...
Kena Biru, Cane Ridge High School: A senior in the health management academy, Kena is part of LEDA (Leadership Enterprise for a Diverse America), a highly regarded organization that helps students ...