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USA approves first gene therapy for rare form of hearing loss
Updated On: 24 April, 2026 01:44 PM IST | Washington | AFP
Developed by the American biotechnology company Regeneron, the treatment known as Otarmeni targets a rare form of hearing loss which affects around 50 newborns a year in the US

Image for representational purpose only. Photo Courtesy: File pic
US health officials on Thursday greenlit a first-of-its-kind gene therapy to treat a rare form of hereditary hearing loss, a breakthrough which could pave the way for other such hearing impairment treatments.
Two to three of every 1,000 children in the United States are born with a hearing impairment, and it is estimated that more than half of these cases of early-onset hearing loss are caused by genetic mutations.
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