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There are several ways in which a hearing loss can be detected. All newborns have a newborn hearing screening and may be referred for a more in-depth hearing test. A child may also be referred by their pediatrician or school nurse when a routine hearing screening indicates more testing is needed. An audiologist conducts a diagnostic hearing test as a first step. This test is more in-depth than a hearing screening.
Depending on the child’s age, there are several options to perform the diagnostic hearing test:
There are many options for hearing loss:
Some hearing losses are genetic. Sensorineural hearing loss is a type of hearing loss caused by damage to the inner ear or auditory nerve. The diagnosis of a sensorineural hearing loss warrants a referral to a genetics specialist, at the family pediatrician’s discretion to rule out genetic syndromes or recessive genetic hearing loss as a reason. It can be caused by a variety of factors, such as abnormalities in the inner ear, a number of viruses and even some medications that are known to cause hearing loss (known as ototoxic medications).
Another type of hearing loss is conductive hearing loss, which can be caused by ear infections, abnormalities in the three small bones in the middle ear, outer ear abnormalities or certain conditions or genetics anomalies. Patients with conductive losses do not receive cochlear implants and there are different options for them.
Finally, there is a type of hearing loss called a mixed hearing loss, which is a combination of the type of hearing losses described above.
Some signs to look out for in children that may indicate hearing loss are:
Every child develops at their own pace and while some speak early and often, others may take longer to develop their speech and language skills. Being aware of common speech and language milestones can help caregivers advocate for their child if they need some extra support.
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