Decoding the Silent Genome: How Precise Phenotyping Revolutionizes Genetic Prediction in Sensorineural Hearing Loss
Sensorineural hearing loss (SNHL) is one of the most prevalent sensory deficits worldwide, affecting hundreds of millions of individuals across all age groups. Caused by structural or functional impairment of the inner ear’s delicate hair cells, the auditory nerve, or central auditory processing pathways, SNHL presents a profound biological and clinical challenge. While genetic mutations … Read more