Delhi woman born with profound hearing loss regains hearing through bilateral cochlear implant, secures admission to IIT ...

A new gene therapy has restored hearing in children and adults with hereditary deafness, according to results from a closely watched clinical trial in China. The treatment targets mutations in the ...

Genetic deficiency of otoferlin, a protein critical to synaptic transmission by the sensory hair cells of the ear, causes congenital deafness. Medicines to treat the condition are lacking; children ...

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'Dada' is a first word for many babies. Babbling sounds with consonant-vowel repetitions, such as 'dada,' are common among infants once they reach 8 months old; however, these sounds are not prevalent ...

Deafness represents a profound hearing loss affecting approximately half a million Americans, creating significant communication challenges. People experiencing deafness might hear absolutely nothing ...

A new therapy for genetic hearing loss has just been approved by the Food and Drug Administration (FDA). The treatment, Otarmeni (lunsotogene parvec-cwha), is the first-ever dual adeno-associated ...

What Is Otarmeni, and Why Does It Matter? Otarmeni (lunsotogene parvec-cwha) is a single-use gene therapy for children and adults who have severe or profound hearing loss (a hearing level of more than ...

Ten children who received DB-OTO for profound genetic hearing loss due to variants of the otoferlin gene showed notable improvements in hearing, according to initial results of the CHORD trial. The ...

For a long time, deafness has often been misunderstood, fueling segregation against people who are deaf or hard of hearing. In some communities, it is still seen as a curse or divine punishment; in ...

An assembly framework and video to learn about the deaf community and Deaf Awareness Week which is celebrated in May each ...