HIGHLIGHTS
SUMMARY
Arena-with terms such as rights, distribution, expertise, participation, and democracy-has been less considered. In most countries the diagnosis during the first hours of life, or even during pregnancy, is limited to a few diseases, due to the high costs and time required for genetic investigations with classical methods. The scenario, in the common welfare realities, is a problem that is faced with patchy responses according to the contexts of care. Many experts tell the authors that all children with a certain diagnosis of ASD (2% of newborns!) should undergo a genetic screening . . .
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