Hearing Loss Autosomal Dominant 82 C5676948
A genetic hearing loss passed down through families in an autosomal dominant pattern. It affects both males and females equally and can vary in age of onset. Treatment includes hearing aids and other assistive devices.
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.
Warning signs - seek immediate care
Vertigo
Facial nerve weakness
Generalized symptoms
(otolaryngologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Sensorineural hearing loss
(otolaryngologic)Tinnitus
(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
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Genetic Counseling Referral
Specialized consultation to explain autosomal dominant inheritance patterns, family risk implications, and reproductive considerations.
Noise Protection Strategies
Education and provision of hearing protection devices to prevent additional noise-induced hearing loss superimposed on genetic loss.
Additional treatment options
Cochlear Implant Candidacy Assessment
Comprehensive evaluation for patients with moderate hearing loss who may progress, determining potential benefit from cochlear implantation if hearing deteriorates.
procedureHerbal and Nutritional Consultation
Assessment of dietary factors and potential supplements that may support auditory health, though evidence remains limited.
complementaryFamily Systems Therapy
Counseling addressing communication patterns, family adjustment, and support mechanisms for living with progressive genetic hearing loss.
psychologicalWhen 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 82 C5676948?
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.
Matsunaga T, Saga K, Kada Y. Clinical practice guidelines for genetic testing in hereditary hearing loss. Auris Nasus Larynx. 2021.
Yasuda M, Chen S, Rodriguez-Buritica D. Molecular genetics of autosomal dominant nonsyndromic hearing loss: An update. Int J Pediatr Otorhinolaryngol. 2020.
Kimura H, Saito Y, Fujita C. Phenotype-genotype correlation in families with autosomal dominant hearing loss. Otol Neurotol. 2019.
Nakano A, Iwasa Y, Hidaka H. Cochlear implantation outcomes in patients with hereditary hearing loss: A systematic review. Clin Otolaryngol. 2022.
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