Story perspectives

Thailand's Newborn Screening Boosts Hearing Loss Diagnosis

9/27/2025

Summary

Story summary

Whole exome sequencing (WES) improves diagnosis of prelingual sensorineural hearing loss (SNHL) in Thailand, identifying MYO7A and MYO15A variants in sporadic and familial cases.
Systematic phenotyping with genetic analysis improves clinical management and counseling for families.
The study urges periodic review of variants as new phenotypes emerge.
Universal newborn hearing screening became Thailand's 2022 public health policy, boosting early detection.

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Story summary

Whole exome sequencing (WES) improves diagnosis of prelingual sensorineural hearing loss (SNHL) in Thailand, identifying MYO7A and MYO15A variants in sporadic and familial cases.
Systematic phenotyping with genetic analysis improves clinical management and counseling for families.
The study urges periodic review of variants as new phenotypes emerge.
Universal newborn hearing screening became Thailand's 2022 public health policy, boosting early detection.