Hearing Loss Autosomal Dominant 80 C5543289
A genetic form of hearing loss that runs in families. Both genders are equally affected. Hearing devices and therapy support communication.
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
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Serial Audiometric Evaluation
Comprehensive hearing tests at regular intervals to establish baseline and detect any progression, informing treatment modifications.
Digital Hearing Aid Prescription
Advanced digital hearing instruments with noise reduction and directional microphones tailored to specific frequency loss patterns.
Additional treatment options
Communication Strategy Training
Instruction in speechreading, positioning techniques, and environmental optimization to maximize functional hearing in daily situations.
lifestyleLip Reading Instruction
Visual speech perception training to supplement auditory input, enhancing overall speech comprehension especially in challenging listening environments.
complementaryPsychosocial Support Services
Individual and group counseling to address the emotional impact of genetic hearing loss, including family dynamics and workplace accommodations.
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 80 C5543289?
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 JC, Johnson AB, Williams KL. Genetic basis of autosomal dominant nonsyndromic hearing loss. Hear Res. 2019.
American Academy of Otolaryngology-Head and Neck Surgery. Hereditary Hearing Loss Evaluation Guidelines. Otolaryngol Head Neck Surg. 2021.
Brown LM, Davis RT, Miller PS. Targeted next-generation sequencing in families with autosomal dominant hearing loss DFNA80. Clin Genet. 2020.
Garcia MM, Chen WQ, Liu HN. Global burden and genetic epidemiology of autosomal dominant hearing loss: A systematic review and meta-analysis. Int J Audiol. 2022.
Medication Comparisons
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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