Universal newborn screening: A roadmap for action
- PMID: 29884465
- DOI: 10.1016/j.ymgme.2018.04.009
Universal newborn screening: A roadmap for action
Erratum in
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Corrigendum to Universal newborn screening: A roadmap for action molecular genetics and metabolism 124 (2018) 177-183.Mol Genet Metab. 2019 Jul;127(3):216-217. doi: 10.1016/j.ymgme.2019.04.009. Epub 2019 Jun 20. Mol Genet Metab. 2019. PMID: 31230977 No abstract available.
Abstract
Newborn screening (NBS) prevents morbidity and mortality by screening babies for selected disorders in the first days of life so that early diagnosis and treatment can be initiated. Congenital disorders impact an estimated 8 million or 6% of annual births worldwide, and of the top five that contribute 25% to the global burden of these disorders, three can be identified and managed by NBS. There are determined pockets of activity in Latin America, Sub-Saharan Africa, and the Asia Pacific region, where partnerships among government, non-governmental organizations, academia, the private sector and civil society are developing novel NBS programs that are both saving lives and preventing disability in those who survive.
Copyright © 2018 Elsevier Inc. All rights reserved.
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