A groundbreaking gene therapy in the UK has changed the life of a young boy with hearing loss. 18-month-old Opal Sandy was born with congenital hearing impairment due to a genetic condition called auditory neuropathy, which disrupts nerve impulses in the inner ear. But thanks to an innovative gene therapy, Sandy’s hearing has been restored.
Opal Sandy’s Treatment Process
The operation for Opal Sandy took just 16 minutes, during which time a working copy of the defective gene was injected into her cells using a harmless virus. This was done directly in Sandy’s ear and a cochlear implant was placed in her left ear. Cochlear implants are common devices used in many people with hearing loss.
Impressive Results of Treatment
After successful treatment, Sandy was soon able to hear loud noises and even applause in her right ear. After six months, the full effect of the treatment was observed and Sandy could now hear almost perfectly without the use of a device. The baby’s hearing improved so much that he could even hear whispers and say words like “Mommy” and “Daddy”.
This success story has also excited doctors at Cambridge University hospitals. In the statement made, it was stated that the new gene therapy is very promising in the treatment of hearing loss and that a new era can be entered in this field. Sandy’s family expressed their happiness, unable to believe the developments. This treatment offers hope for other children with similar conditions in the future.
