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Autosomal Dominant Nonsyndromic Hearing Loss 7 C1832379

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

An inherited hearing condition that may worsen over time, passed directly from an affected parent. Hearing aids and communication therapy support those affected.

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)

Progressive hearing loss

(otolaryngologic)

Bilateral hearing impairment

(otolaryngologic)

Tinnitus

(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

Exercise prescription and weight management

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Hearing Aid Fitting

Application of appropriately programmed hearing aids selected based on comprehensive audiometric assessment to amplify sounds and improve speech comprehension for individuals with mild to moderate hearing loss.

lifestyle
3

Regular Audiological Monitoring

Scheduled hearing assessments every 6-12 months to track disease progression and adjust intervention strategies as hearing thresholds change over time.

monitoring

Additional treatment options

Cochlear Implant Evaluation

Comprehensive surgical candidacy assessment including imaging, audiologic testing, and neural response measurement for patients meeting criteria for cochlear implantation.

procedure

Auditory Rehabilitation Therapy

Structured speech-language therapy focusing on auditory training, lip-reading skills, and communication strategies to maximize functional hearing abilities.

physical_therapy

Ototoxic Exposure Avoidance

Lifestyle modifications eliminating exposure to medications and chemicals known to damage hearing, including certain antibiotics, chemotherapy agents, and industrial solvents.

lifestyle

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 Autosomal Dominant Nonsyndromic Hearing Loss 7 C1832379?

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 JP, Johnson KL, Williams RD. Consensus guidelines for the genetic evaluation of hearing loss. Genet Med. 2022.

guideline2022
2

Brown AB, Davis MN, Anderson PJ. Molecular genetics of autosomal dominant nonsyndromic hearing loss. Hear Res. 2021.

review2021
3

Garcia SR, Chen L, Martinez HV, Thompson KW. Targeted next-generation sequencing in patients with hereditary hearing impairment. JAMA Otolaryngol. 2020.

clinical_trial2020
4

Lee YH, Patel U, Campbell NF, Jackson RT. Systematic review and meta-analysis of cochlear implantation outcomes in hereditary hearing loss. Otol Neurotol. 2023.

meta_analysis2023

Medication Comparisons

Compare medications used to treat Autosomal Dominant Nonsyndromic Hearing Loss 7 C1832379. 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