What is Hearing Loss?
Hearing loss in children can be present at birth (congenital) or develop later inchildhood (acquired). Congenital hearing loss can be hereditary (genetic) or caused by infections during pregnancy, including infection with cytomegalovirus or rubella. Hearing loss is more common in babies who are in the Neonatal Intensive Care Unit (NICU). Hearing loss can be an isolated condition or a feature of a syndrome that causes additional symptoms. Genetic testing can help determine the cause of hearing loss in some cases. Acquired hearing loss can be caused by infectious diseases such as meningitis or recurrent ear infections, as well as trauma and certain medications.
Depending on its cause and origin, the hearing loss can be:
- Sensori-neural, a permanent type of hearing loss which occurs when the inner ear (cochlea) or the auditory nerve is damaged or malformed
- Conductive, which occurs when the sound can’t travel through the ear because of earwax build-up, a foreign body lodged somewhere in the ear, build-up of fluid or a punctured eardrum. Conductive hearing losses may be treated in some cases with medicine or surgery.
Hearing loss is categorized as mild, moderate, severe or profound depending on its severity.
- Reduced hearing, such as inability to hear faint sounds
- Failure to respond to sound
- Delay of language and speech development in young children
- Unclear speech
A hearing test is the best way to diagnose hearing loss and its severity. More tests may be needed to identify the cause. No child is too young to have a hearing test!
Newborns should be tested for hearing loss and deafness shortly after birth in order to start receiving therapy promptly, since intervention within the first six months can prevent developmental and social problems.
- Hearing aids
- Cochlear implants
When to Call for Help
If you see any of the above symptoms in your child, talk to your pediatrician.
At Hopkins Children’s, hearing loss is treated by the Division of Pediatric Otolaryngology.