Observational study shows genetic screening improves early diagnosis of hearing loss in neonates, suggesting timely interventions are critical.
The carrier rates of deafness-related gene mutations in South China were determined. Additionally, certain high-risk neonates developed HL and benefited from follow-up and intervention. Genetic screening can improve early diagnosis and facilitate identification of late-onset cases, resulting in timely clinical recommendations.
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Gu et al. (2025) studied this question.
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