These newborn screening fact sheets were developed by the Committee on Genetics of the American Academy of Pediatrics (AAP) with considerable assistance and consultation from many individuals. It is hoped that the information contained in these fact sheets will assist the pediatrician in understanding the individual tests, their characteristics, and their strengths and weaknesses. Newborn screening is an individual function of each state; therefore, screening programs are not uniform throughout the United States (Table). Because the test results can affect children and parents in a variety of ways, there are special concerns about how states make decisions to adopt new tests and how they evaluate their current screening panels. Currently, many states are examining their practices. The informatiion in the fact sheets was not designed to advocate specific newborn screening tests but to assist pediatricians in evaluating policies and procedures and in developing appropriate positions based on the needs of their patients and their geographic regions.
The following policy statements are a revision:
This article has been cited by other articles:
![]() |
C. E. Mercier, S. E. Barry, K. Paul, T. V. Delaney, J. D. Horbar, R. C. Wasserman, P. Berry, and J. S. Shaw Improving Newborn Preventive Services at the Birth Hospitalization: A Collaborative, Hospital-Based Quality-Improvement Project Pediatrics, September 1, 2007; 120(3): 481 - 488. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. C. Lussky and R. F. Cifuentes False Positive Newborn Screens Secondary to a Maternal Inborn Error of Metabolism Clinical Pediatrics, June 1, 2006; 45(5): 471 - 474. [PDF] |
||||
![]() |
J. R. Botkin, E. W. Clayton, N. C. Fost, W. Burke, T. H. Murray, M. A. Baily, B. Wilfond, A. Berg, and L. F. Ross Newborn Screening Technology: Proceed With Caution Pediatrics, May 1, 2006; 117(5): 1793 - 1799. [Full Text] [PDF] |
||||
![]() |
T. C. Davis, S. G. Humiston, C. L. Arnold, J. A. Bocchini Jr, P. F. Bass III, E. M. Kennen, A. Bocchini, D. Williams, P. Kyler, and M. Lloyd-Puryear Recommendations for Effective Newborn Screening Communication: Results of Focus Groups With Parents, Providers, and Experts Pediatrics, May 1, 2006; 117(5/S1): S326 - S340. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. R. Botkin Research for Newborn Screening: Developing a National Framework Pediatrics, October 1, 2005; 116(4): 862 - 871. [Abstract] [Full Text] [PDF] |
||||
![]() |
N J Kerruish and S P Robertson Newborn screening: new developments, new dilemmas J. Med. Ethics, July 1, 2005; 31(7): 393 - 398. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. S. Wagener States urged to consider newborn screening for cystic fibrosis AAP News, September 1, 2004; 25(3): 124 - 125. [Full Text] [PDF] |
||||
![]() |
L. F. Ross Genetic Exceptionalism vs. Paradigm Shift: Lessons from HIV J. Law Med. Ethics, June 1, 2001; 29(2): 141 - 148. [PDF] |
||||
![]() |
Committee on Bioethics Ethical Issues With Genetic Testing in Pediatrics Pediatrics, June 1, 2001; 107(6): 1451 - 1455. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Brosnan, P. G. Brosnan, J. M. Swint;, J. L. Frias, L. S. Levine, S. E. Oberfield, S. Pang, and J. Silverstein Analyzing the Cost of Neonatal Screening for Congenital Adrenal Hyperplasia Pediatrics, May 1, 2001; 107(5): 1238 - 1238. [Full Text] |
||||
![]() |
L. F. Ross Genetic Exceptionalism vs. Paradigm Shift: Lessons from HIV J. Law Med. Ethics, March 1, 2001; 29(1): 141 - 148. [PDF] |
||||
![]() |
Update: Newborn Screening for Sickle Cell Disease--California, Illinois, and New York, 1998 JAMA, September 20, 2000; 284(11): 1373 - 1374. [Full Text] [PDF] |
||||
![]() |
L. F. Ross and M. R. Moon Ethical Issues in Genetic Testing of Children Arch Pediatr Adolesc Med, September 1, 2000; 154(9): 873 - 879. [Full Text] [PDF] |
||||
![]() |
E. W. Naylor and D. H. Chace Automated Tandem Mass Spectrometry for Mass Newborn Screening for Disorders in Fatty Acid, Organic Acid, and Amino Acid Metabolism J Child Neurol, November 1, 1999; 14(1_suppl): S4 - S8. [Abstract] [PDF] |
||||
![]() |
C. Meyer, J. Witte, A. Hildmann, K.-H. Hennecke, K.-U. Schunck, K. Maul, U. Franke, H. Fahnenstich, H. Rabe, R. Rossi, et al. Neonatal Screening for Hearing Disorders in Infants at Risk: Incidence, Risk Factors, and Follow-up Pediatrics, October 1, 1999; 104(4): 900 - 904. [Abstract] [Full Text] |
||||
![]() |
A. A. Reilly, R. Bellisario, and K. A. Pass Multivariate discrimination for phenylketonuria (PKU) and non-PKU hyperphenylalaninemia after analysis of newborns' dried blood-spot specimens for six amino acids by ion-exchange chromatography Clin. Chem., February 1, 1998; 44(2): 317 - 326. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. Mehl and V. Thomson Newborn Hearing Screening: The Great Omission Pediatrics, January 1, 1998; 101 (1): e4 - e4. [Abstract] [Full Text] [PDF] |
||||