Does every baby get a newborn screening test?

We should do all we can to ensure that every baby benefits from this important preventive activity

Biochemical Genetics and Newborn Screening Services, The Children's Hospital at Westmead, Westmead, NSW.

Correspondence:

1. Wilcken B, Wiley V, Hammond J, Carpenter K. Screening newborns for inborn errors of metabolism by tandem mass spectrometry. N Engl J Med 2003; 348: 2304-2312.
2. Metz MP, Ranieri E, Gerace RL, et al. Newborn screening in South Australia: is it universal? Med J Aust 2003; 179: 412-415.<eMJA full text>
3. Ades AE, Walker J, Jones R, Smith I. Coverage of neonatal screening: failure of coverage or failure of information system. Arch Dis Child 2001; 84: 476-479.
4. Wake MA. Newborn hearing screening: decision time for Australia. Med J Aust 2002; 177: 172-173. <eMJA full text>
5. Meikle PJ, Ranieri E, Ravenscroft EM, et al. Newborn screening for lysosomal storage disorders. Southeast Asian J Trop Med Public Health 1999; 30 Suppl 2: 104-110.
6. Davis DS. Genetic dilemmas and the child’s right to an open future. Hastings Cent Rep 1997; 27(2): 7-15.

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