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Hearing Loss Autosomal Dominant 78 C5436768

Published: July 22, 2026Updated: August 20, 2026

An autosomal dominant hearing loss condition. Family history is often present. Amplification devices and communication training are helpful.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

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

1

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

1

Bilateral Hearing Aid Provision

Fitting of hearing aids for both ears to provide balanced hearing and improved localization. Includes verification procedures and user training.

procedure
2

Healthy lifestyle changes and stress management

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
3

Comprehensive Auditory Training

Structured program developing skills in sound discrimination, speech perception, and communication strategies. Uses individualized exercises and progress monitoring.

physical_therapy

Additional treatment options

Tinnitus Management Techniques

Sound therapy and counseling for associated tinnitus symptoms common in genetic hearing loss. Includes white noise devices and relaxation training.

complementary

Annual Hearing Threshold Tracking

Systematic documentation of hearing levels over time to detect any progression requiring treatment modification. Includes both air and bone conduction testing.

monitoring

Family Education Program

Structured education for family members about hearing loss management, effective communication techniques, and supporting the affected individual's wellbeing.

psychological

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Hearing Loss Autosomal Dominant 78 C5436768?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Smith JM, Johnson KL, Williams RD. Clinical practice guidelines for genetic evaluation of autosomal dominant hearing loss. Otolaryngol Head Neck Surg. 2022.

guideline2022
2

Patel N, Chen Y, Martinez MH, Lee SH. Molecular mechanisms of autosomal dominant nonsyndromic hearing loss. Hear Res. 2021.

review2021
3

Anderson PC, Thompson RJ, Garcia-Lopez A. Efficacy of hearing rehabilitation in autosomal dominant hearing loss: a prospective cohort study. JAMA Otolaryngol Head Neck Surg. 2020.

clinical_trial2020
4

Roberts CJ, Kim DW, Brown NA, Nguyen HT. Genetic heterogeneity in autosomal dominant hearing loss: a systematic review and meta-analysis. Clin Genet. 2023.

meta_analysis2023

Medication Comparisons

Compare medications used to treat Hearing Loss Autosomal Dominant 78 C5436768. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy