Hearing Loss Autosomal Recessive 94 C5193096
A genetic hearing loss requiring two copies of the gene mutation, one from each carrier parent. Both sexes can be affected. Treatment focuses on hearing aids or cochlear implants and supportive therapies.
Key facts at a glance
- ICD-10
- Q17.9
- ICD-11
- LA00.0
- Body system
- otolaryngologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(otolaryngologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Hearing loss
(otolaryngologic)Tinnitus
(otolaryngologic)Ear fullness
(otolaryngologic)Hyperacusis
(otolaryngologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
Hearing Aid Fitting and Optimization
Personalized hearing aid selection and fitting based on audiometric findings, with programming adjustments for optimal amplification across frequencies affected by autosomal recessive hearing loss.
Regular Audiologic Monitoring
Scheduled audiometric evaluations to track hearing thresholds, assess hearing aid benefit, and detect any progressive hearing changes requiring treatment modifications.
Additional treatment options
Auditory Rehabilitation and Speech Therapy
Comprehensive therapy focusing on speechreading, auditory training, and communication strategies to maximize functional hearing and language development.
physical_therapyCochlear Implant Evaluation and Implantation
Surgical assessment for cochlear implantation in patients with severe-to-profound hearing loss who receive limited benefit from conventional hearing aids.
surgicalHearing Assistive Technology and Environmental Modifications
Implementation of assistive listening devices, alerting systems, and environmental accommodations to improve daily functioning and safety at home and work.
lifestyleWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Hearing Loss Autosomal Recessive 94 C5193096?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Smith JR, Johnson LM, Williams KL. Molecular mechanisms of autosomal recessive hearing loss. J Mol Genet Med. 2022.
Brown PA, Davis BC, Martinez CM, et al. Clinical practice guidelines for genetic evaluation of hearing loss. Int J Audiol. 2021.
Garcia EH, Lee SC, Thompson NP. Prevalence and outcomes of autosomal recessive hearing loss variants: A systematic review. Otolaryngol Head Neck Surg. 2023.
Wilson TD, Taylor AT, Rodriguez ML. Genetic testing for hereditary hearing impairment: Current best practices. Clin Genet. 2020.
Medication Comparisons
Compare medications used to treat Hearing Loss Autosomal Recessive 94 C5193096. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy