For example, in New Zealand, galactosemia, congenital adrenal hyperplasia, biotinidase deficiency, cystic fibrosis (CF) and maple syrup urine disease were see more successively added to the list of screening conditions, over the 1970s and 1980s (National Testing Centre 2010). In other countries, opportunities were taken to add additional tests to the screening programme such as Protein Tyrosine Kinase inhibitor haemoglobinopathies as a result of high carrier rates in specific populations (Benson and Therrell 2010; Streetly and

Dick 2005). However, prior to expanded screening on an international basis, the number of tests in each health system or US state ranged from as few as two or three up to seven (Watson et al. 2006). During the1990s, advances in technology led to the development of tandem mass spectrometry, with the capacity to accurately screen for a much larger number of rare metabolic diseases (Hill 1993; Jones and Bennett 2002; Röschinger Selleckchem VX-765 et al. 2003). By 2007, screening was underway for an average of about 27 metabolic disorders throughout most US states, parts of Canada and all of Australia and New Zealand (Sharrard and Pollitt 2007). In contrast, despite a modest increase in screening targets

in Britain and other parts of Canada, there are still considerably fewer tests offered by so-called expanded screening programmes. There is substantial literature that is either supportive (Tarini 2007; Avard et al. 2007; Lin and Fleischman 2008; Alexander and van Dyck 2006; Howell 2006) Temsirolimus mouse or critical/cautious about expanded

newborn screening (Bailey and Murray 2008; Moyer et al. 2008; Grosse et al. 2006; Botkin et al. 2006). Internationally, some jurisdictions are noted for their prompt uptake of the associated technologies, with others slow and seemingly reluctant to follow the trend (Green et al. 2006; Padilla et al. 2010). Adding to the contention about further expansion of screening is debate about how to respond to technological advancement that makes it technically possible to screen for Fragile X (Bailey and Murray 2008; Coffee et al. 2009), lysosomal storage diseases (Li et al. 2004; Meikle et al. 2006), immune deficiencies (Cassol et al. 1994; Puck 2007), Duchenne muscular dystrophy (Parsons and Bradley 2008; van Ommen and Scheuerbrandt 1993) and other rare disorders (Röschinger et al. 2003). Differentials in the uptake of disorders into screening programmes are suggestive of discrepancies between screening criteria and a lack of international standardization (Tuuminen et al. 1994). The development of screening programmes and the differences that have evolved are the consequence of context-specific interpretations of and amendments to screening criteria (Clague and Thomas 2002; Padilla et al. 2010). Moreover, they are also dictated by financial resources, incidence rate, the strength of patient advocacy and cultural differences (Pollitt 2007).