Krabbe newborn screening: The issue of informed consent

Public Health Ethics

Volumn 6, Issue 1, 2013, Pages 126-128

  Nijsingh, Niels ^a  

^a UTRECHT UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

GLOBOID CELL LEUKODYSTROPHY; HEALTH CARE POLICY; HUMAN; INFORMED CONSENT; NEWBORN SCREENING; PARENTAL CONSENT; PRIORITY JOURNAL; REVIEW; STEM CELL TRANSPLANTATION;

EID: 84875608647     PISSN: 17549973     EISSN: 17549981     Source Type: Journal    
DOI: 10.1093/phe/pht009     Document Type: Review

References (5)

1. Dees, R. and Kwon, J. (2013). The Ethics of Krabbe Screening. Public Health Ethics, 6, 114-119.
2. Nijsingh, N. (2007). Informed Consent and the Expansion of Newborn Screening. In Dawson, A. and Verweij, M. (eds), Ethics, Prevention, and Public Health. Oxford: Oxford University Press, pp. 198-212.
3. Nijsingh, N. (2012). Blurring Boundaries. The American Journal of Bioethics, 12, 26-27.
4. Ross, L. F. (2006). Screening for Conditions that Do Not Meet the Wilson and Jungner Criteria: The Case of Duchenne Muscular Dystrophy. American Journal of Medical Genetics, 140, 914-922.
5. Wilson, J. M. and Jungner, Y. G. (1968). Principles and Practice of Screening for Disease. Geneva: World Health Organization.