Advancing Neonatal Genetic Screening For Better Outcomes
Received Date: Oct 02, 2025 / Published Date: Oct 30, 2025
Abstract
Neonatal genetic screening has advanced with expanded programs utilizing technologies like tandem mass spectrometry, DNA
analysis, WES, and NGS for early detection of inherited disorders. Early diagnosis improves outcomes through timely interventions.
Genomic sequencing offers comprehensive genetic insights for rare diseases. Ethical considerations, data interpretation, follow-up
care, and equitable access remain challenges. Successful SCID screening demonstrates the potential of proactive genetic testing,
though cost-effectiveness requires attention.
Citation: Al-Masri DH (2025) Advancing Neonatal Genetic Screening For Better Outcomes. NNP 11: 588.
Copyright: 聽漏 2025 Dr. Hana Al-Masri This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permitsunrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
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