Hearing Loss Autosomal Dominant 85 C5774302
A hereditary hearing condition following an autosomal dominant inheritance pattern. It can affect anyone regardless of gender and varies in severity. Treatment focuses on hearing aids and rehabilitation strategies.
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 spells
Facial paresis
Generalized symptoms
(otolaryngologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
High-frequency 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
Hearing Aids
Prescription hearing aids fitted by an audiologist to amplify sounds and improve speech comprehension. Regular follow-up adjustments are needed to optimize settings as hearing needs evolve.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Regular Audiological Monitoring
Scheduled hearing assessments every 6-12 months to track progression of hearing loss and adjust intervention strategies accordingly.
Additional treatment options
Auditory Rehabilitation Therapy
Speechreading and auditory training exercises to improve communication skills and help patients maximize residual hearing abilities.
physical_therapyBone Anchored Hearing System Evaluation
Assessment for bone-anchored hearing devices that bypass the outer and middle ear to directly stimulate the inner ear through bone conduction.
procedureCommunication Strategies Training
Education on effective communication techniques including positioning, lighting, and environmental modifications to enhance listening in daily situations.
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 Hearing Loss Autosomal Dominant 85 C5774302?
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-Jones KB, Williams RJ, Chen LM. Clinical practice guidelines for genetic hearing loss syndromes. Otolaryngol Head Neck Surg. 2022.
Garcia-Marquez A, Thompson PD, Patel R. Advances in understanding autosomal dominant hearing loss. Hear Res. 2021.
Anderson CF, Liu Y, Nakamura T. Genetic modifiers in DFNA hearing loss: a prospective cohort study. JAMA Otolaryngol Head Neck Surg. 2020.
Brown HM, Rodriguez-Vargas MP. Molecular genetics of nonsyndromic hearing loss. In: Current Topics in Otology. 2023.
Medication Comparisons
Compare medications used to treat Hearing Loss Autosomal Dominant 85 C5774302. 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