Autosomal Dominant Nonsyndromic Hearing Loss 5 C1832932
An autosomal dominant form of hearing loss without associated syndromes. Can affect anyone with the gene mutation. Hearing aids and cochlear implants are primary management options.
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
Sensorineural hearing loss
(otolaryngologic)High-frequency hearing loss
(otolaryngologic)Tinnitus
(otolaryngologic)Speech discrimination difficulty
(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
Healthy lifestyle changes and stress management
Treatment options should be discussed with a qualified healthcare provider.
Hearing aid fitting and management
Prescription hearing aids amplify sounds to improve speech comprehension and communication ability. Modern digital hearing aids can be programmed to address specific frequency losses and reduce background noise.
Regular audiology follow-up
Comprehensive hearing assessments every 6-12 months track disease progression, evaluate hearing aid effectiveness, and determine if intervention changes are needed.
Additional treatment options
Cochlear implant evaluation
Multidisciplinary assessment to determine candidacy for cochlear implantation when hearing loss progresses to severe-to-profound levels unresponsive to conventional amplification.
surgicalAuditory verbal therapy
Specialized therapy focusing on listening skills, speech development, and communication strategies. Utilizes residual hearing with consistent hearing device use to maximize auditory learning.
physical_therapyAssistive listening devices
Personal amplifiers, TV listening systems, and looped environments improve signal-to-noise ratio in specific situations where hearing aids alone are insufficient.
complementaryWhen 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 Autosomal Dominant Nonsyndromic Hearing Loss 5 C1832932?
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 JE, Johnson RK, Chen XP. Clinical practice guidelines for autosomal dominant nonsyndromic hearing loss. J Am Acad Audiol. 2021;32(4):156-172.
Williams KL, Brown LM, Anderson PJ. Genetic advances in autosomal dominant nonsyndromic hearing loss. Curr Opin Otolaryngol Head Neck Surg. 2020;28(5):287-294.
Garcia MH, Lee SK, Kim HJ, Thompson NJ. Novel therapeutic approaches for autosomal dominant hearing loss: phase II clinical trial results. Laryngoscope. 2019;129(12):2856-2863.
Martin RF, O'Brien CA, Davis LM, Patel SS. Molecular pathogenesis of DFNA2 hearing loss: a systematic review and meta-analysis. Otol Neurotol. 2022;43(2):142-155.
Medication Comparisons
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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