Hearing loss can run in families, though you may not be as susceptible as your relatives. At Joy Hearing Health Clinic on Sprucewood Avenue in LaSalle, audiologist Adefunke Sabageh, Au.D., and hearing instrument specialist OJ Sabageh, HIS, can evaluate your hearing with your family history in mind and help you understand how genetics may affect your hearing health. If hearing loss is a known condition in your family, early testing and protective habits can help you preserve your hearing and address changes sooner.
Which Forms of Hearing Loss Are Considered Genetic?
Hearing loss is considered genetic when it’s caused by changes in genes that affect how the ear develops or functions. Most genetic hearing loss is sensorineural, meaning it involves the hair cells of the inner ear or the auditory nerve. It may be present at birth or develop later in life.
Genetic hearing loss is generally split into two categories. Nonsyndromic hearing loss accounts for about 70% of genetic cases and occurs without other medical symptoms. Syndromic hearing loss makes up the remaining 30% and occurs alongside other health conditions, such as Usher, Pendred, and Waardenburg syndromes.
How Are Hearing Loss Genes Passed From One Generation to the Next?
Hearing loss genes are passed from one generation to the next through specific inheritance patterns, and the pattern determines each child’s risk. Depending on the pattern, a child’s chance may range from no risk to 50% or higher, and in many cases, parents with normal hearing can still have a child with genetic hearing loss.
The main inheritance patterns include:
- Autosomal dominant: Only one changed gene from one parent is needed, giving each child a 50% chance of inheriting the condition.
- Autosomal recessive: Both parents carry one changed gene without having hearing loss themselves, giving each child a 25% chance of inheriting the condition.
- X-linked: The changed gene is on the X chromosome, so males are more likely to be affected, while females are often carriers.
- Mitochondrial: The condition is passed only by the mother and can affect all of her children.
Autosomal recessive inheritance accounts for about 80% of nonsyndromic genetic hearing loss, which explains why most infants with hearing loss are born to parents with normal hearing. Even within the same family, severity and age of onset can vary from one person to another.
Does Hereditary Hearing Loss Start in Infancy or Later in Life?
Hereditary hearing loss can start in infancy, or it can develop during childhood or later in adulthood. Some forms are congenital and identified through newborn hearing screening, while others are progressive and develop gradually over years or decades.
Congenital hearing loss affects up to three in every 1,000 babies, and inherited genetic factors contribute to about 60% of hearing loss in infants. In young children, signs may include not reacting to loud sounds, not turning toward voices, or delays in speech and language development.
Later-onset genetic hearing loss often develops slowly, which can make it easy to overlook. Adults may notice:
- Difficulty following conversations in noisy places
- Asking others to repeat themselves
- Turning up the television or phone volume
- Ringing or buzzing in the ears
Because gradual changes can go unnoticed, family members are often the first to recognize them.
Why Get a Baseline Hearing Test if Your Relatives Have Hearing Loss?
A baseline hearing test gives you a reference point if your relatives have hearing loss, and regular evaluations can catch changes even before symptoms appear. You should also have your hearing tested as soon as you notice changes.
Almost all hospitals screen newborns for hearing loss within the first few days of life. Children who pass newborn screening but have a family history of hearing loss may still benefit from monitoring, since some genetic forms develop later.
For adults, a baseline hearing evaluation provides a reference point for tracking changes over time. Our hearing care team can perform comprehensive hearing testing, discuss your family history, and recommend how often you should return for follow-up testing. When a genetic cause is suspected, Adefunke Sabageh may recommend a referral for genetic counselling or testing. Currently, no genetic test can predict whether a person will develop age-related hearing loss, which makes regular hearing evaluations especially important.
How Can You Keep Your Hearing Healthy With a Genetic Risk?
You can keep your hearing healthy with a genetic risk by limiting noise exposure, using hearing protection, reviewing medications with your healthcare providers, managing your overall health, and scheduling regular hearing evaluations.
Because some genes can make the inner ear more vulnerable to damage, avoiding additional strain is especially important. Wearing earplugs or earmuffs around loud equipment, concerts, or firearms and keeping headphone volume at moderate levels can reduce noise exposure. Some medications can affect hearing, so let your healthcare providers know about a family history of hearing loss before starting new prescriptions.
Overall health also plays a role. Conditions such as high blood pressure, heart disease, and diabetes may increase the risk of hearing loss, so managing these conditions supports long-term hearing health.
When hearing loss does develop, Adefunke Sabageh and OJ Sabageh can recommend options such as hearing aids and track changes over time to adjust your care as needed.
Plan a Hearing Evaluation at Joy Hearing Health Clinic in LaSalle
If hearing loss runs in your family, a hearing evaluation with Adefunke Sabageh or OJ Sabageh is a smart first step. Your first visit establishes a baseline and helps determine whether treatment or continued monitoring makes sense for you.
Call or text 226-400-1866 or contact Joy Hearing Health Clinic to schedule an appointment at our Sprucewood Avenue office in LaSalle, with free parking on site.