Detecting Hearing Impairment in Infants

Globally, 1 to 3 in every 1000 children experience hearing impairments, with some being present at birth (congenital) and others acquired after. In certain nations, such as the US, there’s a mandatory screening for hearing defects starting at 3 months of age. Early detection is crucial, as prompt intervention can successfully treat hearing loss in its initial stages.

Causes for hearing defects in Infants and children?

Several factors can contribute to hearing defects in infants and children. Common causes include genetic factors, exposure to infections during pregnancy, complications during childbirth, and a family history of hearing impairments. Additionally, exposure to loud noises, certain medications, and conditions like meningitis or chronic ear infections can also play a role. Timely identification of these factors and early intervention are crucial in managing and addressing hearing defects in children.

  • Genetic factors: Genetic factors contributing to congenital hearing loss can involve various gene mutations or abnormalities that affect the development and function of the auditory system. Specific genetic syndromes, such as Usher syndrome, Waardenburg syndrome, or Pendred syndrome, may include hearing loss as one of their features. Additionally, non-syndromic genetic hearing loss can occur without other associated conditions.

The inheritance pattern can vary, including autosomal dominant, autosomal recessive, or X-linked forms, depending on the specific genetic mutation. Genetic testing and counseling can help identify the underlying genetic factors, assess the risk of hearing loss, and provide guidance for families.

  • Exposure to certain infections:
  1. Rubella (German measles): Rubella infection during pregnancy can lead to congenital rubella syndrome, which may include hearing impairments among its effects.
  2. Cytomegalovirus (CMV): CMV is a common virus that, if contracted during pregnancy, can lead to congenital CMV infection, potentially causing hearing loss and other developmental issues.
  3. Toxoplasmosis: Toxoplasmosis, caused by the Toxoplasma gondii parasite, can be transmitted from mother to fetus and may result in congenital toxoplasmosis, which can include hearing problems.
  • Non-genetic factors:
  1. Infections during pregnancy: Certain infections, such as rubella (German measles), cytomegalovirus (CMV), and toxoplasmosis, can affect the developing fetus and lead to hearing impairments.
  2. Complications during childbirth: Birth-related factors, including lack of oxygen during delivery (birth asphyxia), premature birth, or low birth weight, can contribute to hearing loss.
  3. Exposure to loud noises: Prolonged exposure to loud noises, both in utero and after birth, can damage the delicate structures of the inner ear and result in hearing loss.
  4. Use of ototoxic medications: Some medications, especially when administered during pregnancy or infancy, can have damaging effects on the auditory system.
  5. Illnesses and infections: Conditions such as meningitis or chronic ear infections, if not promptly treated, can lead to hearing loss in children.


In the initial two years of a child’s life, various factors can contribute to the gradual development of acquired hearing loss. These include:

  • Perforated eardrum: A hole or tear in the eardrum can result in hearing impairment.
  • Severe head injury: Serious trauma to the head may lead to hearing loss.
  • Otosclerosis or Meniere’s diseases: Conditions like otosclerosis or Meniere’s disease can contribute to auditory issues.
  • Infections and diseases: Meningitis, measles, mumps, or whooping cough can impact hearing health.
  • Untreated ear infection: Failure to address conditions like untreated otitis media can lead to hearing loss.
  • Noise-induced hearing loss: Prolonged exposure to loud noise can cause gradual hearing impairment.
  • Second-hand smoke exposure: Being exposed to second-hand smoke is linked to an increased risk of hearing problems.

What are the Types of Hearing loss in Infants?

  • Conductive Hearing Loss: This type occurs when sound waves are unable to pass through the ear canal to the middle ear. It is often associated with earwax buildup, fluid in the middle ear, or structural issues in the ear.
  • Sensorineural Hearing Loss: Sensorineural hearing loss results from damage to the inner ear or the auditory nerve. It can be caused by genetic factors, infections, certain medications, or exposure to loud noises.
  • Mixed Hearing Loss: Mixed hearing loss is a combination of both conductive and sensorineural hearing loss. This means there may be problems with the outer or middle ear as well as damage to the inner ear or auditory nerve.

How do we Screen Infants for Hearing loss?

Infants are typically screened for hearing loss using tests such as:

  • Otoacoustic Emissions (OAE) Test: This test involves placing a small probe in the baby’s ear, which emits sounds. If the baby’s ear is healthy, an echo response, known as an otoacoustic emission, is produced. Lack of response may indicate hearing issues.
  • Auditory Brainstem Response (ABR) Test: This test measures the electrical activity in the auditory nerve and brainstem in response to sounds. Electrodes are placed on the baby’s head to monitor the neural responses.
  • Auditory Steady State Response (ASSR) Test: The ASSR test measures the brain’s steady-state response to auditory stimuli, assessing hearing thresholds across various frequencies, and is commonly employed in infants and individuals with limited responsiveness to traditional hearing tests.
  • Central Auditory Evoked Potential (CAEP) Test: The CAEP test examines the brain’s response to sound stimuli, specifically targeting central auditory pathways, providing insights into auditory information processing and identifying potential issues with auditory processing.
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  • Otoacoustic Emissions (OAE) Test: The OAE test assesses the sounds generated by the inner ear (cochlea) in response to external stimuli, serving as a common method to evaluate cochlear functionality and detect hearing loss or impairment.
  • Tympanometry: Tympanometry is a test that measures the movement of the eardrum in response to changes in air pressure, providing information about middle ear function.
  • Middle ear muscle reflex (MEMR): The Middle Ear Muscle Reflex (MEMR) assesses the contraction of the muscles in the middle ear in response to loud sounds, aiding in the evaluation of auditory sensitivity.

These tests are non-invasive and can be performed while the baby is asleep or resting. Early screening is crucial to identify hearing issues and initiate necessary interventions for optimal development.

In conclusion, Regular ear check-ups for infants are crucial to detect and address potential hearing issues early on. Early intervention can significantly impact a child’s development and ensure optimal communication skills. By identifying and addressing hearing concerns in infancy, we contribute to a child’s overall well-being and lay the foundation for a healthy auditory system.

Nizamiye Hospital, situated in Abuja, stands ever-prepared to provide its esteemed clientele with specialized treatment across a spectrum of health issues. Our dedicated team of medical professionals, boasting an extensive repertoire of over 24 specialized departments, ensures the successful, cost-effective, and efficient management of various healthcare concerns. Located at Plot 113, Sector S, Cadastral Zone, Life Camp, Abuja, Nigeria, we extend a warm invitation for your visit. For inquiries or appointments, feel free to call or text Veno from Public Relations at 08166666023 – 08056339444

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