SUPPLEMENT ARTICLE |
a National Institutes of Health, Bethesda, Maryland
b Health Resources and Services Administration, Rockville, Maryland
In 40 years, newborn screening has evolved to become a standard component of preventive public health. Despite its widespread acceptance, efforts need to be made to overcome some significant problems. There is inequity in the conditions for which states screen routinely, and many conditions that could be screened for are not, for economic or logistic reasons. Existing (tandem mass spectrometry) and potential (DNA microarray) technologies could be developed and put in place to correct these existing shortcomings. To do so will require investment in the technologies, combined with public and professional education and provision of a high-quality, accessible system for confirmation of diagnoses, family counseling, initiation of treatment, and the opportunity to participate in research to develop new or improved therapies.
Key Words: newborn screening recommendations
Abbreviations: NIHNational Institutes of Health HRSAHealth Resources and Services Administration MCHBMaternal and Child Health Bureau NICHDNational Institute of Child Health and Human Development
This article has been cited by other articles:
![]() |
B. Wilfond and L. F. Ross From Genetics to Genomics: Ethics, Policy, and Parental Decision-making J. Pediatr. Psychol., July 22, 2008; (2008) jsn075v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. W. Clayton Incidental findings in genetics research using archived DNA. J. Law Med. Ethics, June 1, 2008; 36(2): 286 - 291. [PDF] |
||||
![]() |
N. J. Kerruish, P. L. Campbell-Stokes, A. Gray, T. R. Merriman, S. P. Robertson, and B. J. Taylor Maternal Psychological Reaction to Newborn Genetic Screening for Type 1 Diabetes Pediatrics, August 1, 2007; 120(2): e324 - e335. [Abstract] [Full Text] [PDF] |
||||