Newborn screening: new developments, new dilemmas

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Newborn screening: new developments, new dilemmas.

Scientific and technological advances are lending pressure to expand the scope of newborn screening. Whereas this has great potential for improving child health, it also challenges our current perception of such programmes. Standard newborn screening programmes are clearly justified by the fact that early detection and treatment of affected individuals avoids significant morbidity and mortality...

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New developments in neonatal screening.

There have been significant advances in the methods available for the detection and investigation of individuals with inherited metabolic disorders. The burgeoning of molecular biology in recent years and the discovery of new classes of inherited metabolic disorders, such as inborn errors of fat oxidation, are well known. What is perhaps less well recognised, is that there have been comparable ...

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New technologies in newborn screening.

In our Supplemental Newborn Screening Program in western Pennsylvania, we have introduced not only a unique approach to newborn screening, but also some innovative concepts in follow-up confirmation and prognostic diagnosis. The Pennsyl-vania Department of Health routinely screens only for phenylketonuria and congenital hypothyroidism. In an attempt to extend this basic state-mandated screening...

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Ethics and Newborn Genetic Screening: New Technologies, New Challenges

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Newborn screening in Australia and New Zealand.

Newborn screening began in Australia and New Zealand in the mid-1960's as local and pilot programs and implemented as country or state-wide programs around 1970. There are five programs covering all Australia and one for New Zealand. All screening programs are fully government funded, as is treatment for the conditions found by the screening programs and newborn screening is a universally adopt...

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ژورنال

عنوان ژورنال: Journal of Medical Ethics

سال: 2005

ISSN: 0306-6800

DOI: 10.1136/jme.2004.008219