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Page 8 of 10    Gonzaga-Jauregui et al. Rare Dis Orphan Drugs J 2024;3:16  https://dx.doi.org/10.20517/rdodj.2024.02

               Mexico and other LAC countries should start considering now how to best implement effective and
               comprehensive ENBS programs for their populations and in their primarily socialized healthcare systems.
               At the same time, governments and health authorities across the region ought to begin considerations for
               the implementation of modern and future early disease detection technologies for population health. While
               the time for adoption and implementation of MS/MS technologies for ENBS may have passed for the
               countries of the region, it is now timely to explore the implementation of the next generation of ENBS
               programs through research pilot projects that can assess their effectiveness and feasibility. Ideally, gNBS
               should be complimentary to metabolic ENBS using MS/MS; however, in countries where ENBS does not
               exist as the standard of care for newborns nationwide, the strategic investment in technologies that can
               maximize the benefit for as many newborns, patients, and families as possible should be considered.


               Not only will this have an impact on improved health and life expectancy outcomes for newborns at risk,
               but it has been proven that early detection of rare genetic diseases is cost-effective for healthcare systems
               and societies in the long term [27-30] . Additionally, the ability to know the prevalence of diseases in local
               populations and the number of patients with conditions for which there is an available treatment can enable
               better national public health planning, budgeting, and price negotiation with pharmaceutical companies for
               improved access to treatments and proper disease management. In healthcare systems marked by limited
               resources and challenging access to new therapeutics for rare diseases, early diagnoses and interventions
               become imperative. Patients treated at advanced stages of a disease are at greater risk of long-term
               complications and disability, which not only profoundly impacts the patients and their families, but also the
               already constrained healthcare budgets and systems in resource-limited countries such as Mexico and those
               in the LAC region.


               DECLARATIONS
               Authors’ contributions
               Made substantial contributions to the conception and writing of the original manuscript: Gonzaga-Jauregui
               C, Moreno-Salgado R, Tovar-Casas J, Navarrete-Martínez JI
               Provided   insightful   comments   and   revised   the   manuscript:   Gonzaga-Jauregui   C,  Tovar-
               Casas J, Navarrete-Martínez JI


               Availability of data and materials
               Not applicable.


               Financial support and sponsorship
               None.


               Conflicts of interest
               All authors declared that there are no conflicts of interest.


               Ethical approval and consent to participate
               Not applicable.


               Consent for publication
               Not applicable.

               Copyright
               © The Author(s) 2024.
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