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Newborn screening enables healthier lives
Recent advances in gene therapy are expected to significantly expand treatment options for rare genetic disorders identified through newborn screening. Early detection and intervention, such as in the case of PKU, can enable children to live normal lives and prevent severe disabilities, highlighting the importance of comprehensive screening programs. However, the high costs of new treatments and the funding challenges for expanding screening panels remain major barriers to widespread implementation.
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تنويه: هذا ملخص تم إنشاؤه بواسطة الذكاء الاصطناعي
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