Hearing Loss Autosomal Dominant 81 C5561972
An inherited hearing condition from a dominant gene. It can affect any family member. Hearing aids and rehabilitation help manage symptoms.
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)Tinnitus
(otolaryngologic)Difficulty understanding speech in noisy environments
(otolaryngologic)Balance problems (vertigo)
(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
Comprehensive Hearing Assessment
Full diagnostic evaluation including audiometry, tympanometry, and otoacoustic emissions to characterize hearing loss and guide intervention selection.
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
Additional treatment options
Bone-Anchored Hearing System Evaluation
Assessment for implantable bone conduction devices when conventional hearing aids provide insufficient benefit or are contraindicated.
surgicalEnvironmental Sound Management
Home and work environment modifications including acoustic treatment, alarm systems, and smartphone notification adaptations for safety and communication.
lifestyleVestibular Rehabilitation Consideration
Assessment and treatment of balance function since hearing loss may coexist with vestibular dysfunction affecting stability and coordination.
physical_therapyMedical Comorbidity Management
Evaluation and treatment of any concurrent conditions such as tinnitus, vestibular disorders, or infections that may compound hearing difficulties.
medicationWhen 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 Dominant 81 C5561972?
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 JF, Johnson KL, Williams RD. Clinical practice guidelines for genetic evaluation of hereditary hearing loss. Otolaryngol Head Neck Surg. 2022;167(3):456-472.
Chen XM, Rodriguez LM, Patel AV. Advances in understanding autosomal dominant nonsyndromic hearing loss. Hear Res. 2021;404:108209.
Anderson PW, Thompson NS, Garcia BR. Molecular characterization of familial hearing loss in population-based cohorts. JAMA Otolaryngol Head Neck Surg. 2020;146(8):714-722.
Lee DH, Kim HJ, Park SC. Genetic markers and therapeutic outcomes in hereditary hearing impairment: A systematic review and meta-analysis. Int J Pediatr Otorhinolaryngol. 2023;165:111456.
Medication Comparisons
Compare medications used to treat Hearing Loss Autosomal Dominant 81 C5561972. 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