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Autosomal Recessive Nonsyndromic Hearing Loss 79 C2750082

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

A genetic condition causing profound hearing loss from birth. It is passed when both parents carry the gene. Cochlear implants and speech therapy are common treatments.

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
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Sudden hearing loss

Generalized symptoms

(otolaryngologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Hearing loss

(otolaryngologic)

Tinnitus

(otolaryngologic)

Balance disturbances

(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

Cochlear Implantation

Surgical placement of an electronic device that bypasses damaged hair cells and directly stimulates the auditory nerve. Requires comprehensive pre-operative evaluation including imaging and hearing assessments.

surgical
2

Medication management with follow-up

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Bone-Anchored Hearing System

Surgically implanted or soft-band worn device that transmits sound through bone conduction, useful when traditional hearing aids are not suitable.

lifestyle

Additional treatment options

Educational Support Services

School-based services including individual education plan development, classroom accommodations, and liaison with teachers to ensure appropriate academic support.

psychological

Auditory Rehabilitation Program

Comprehensive therapy program combining hearing device use with training in speech reading, listening strategies, and communication tactics.

physical_therapy

Regular ENT Follow-up

Periodic evaluations with otolaryngology specialists to monitor hearing status, assess device function, and evaluate for any syndromic features or complications.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Autosomal Recessive Nonsyndromic Hearing Loss 79 C2750082?

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 JR, Johnson LA, Williams KD. Clinical practice guidelines for genetic hearing loss evaluation. J Audiol Med. 2022.

guideline2022
2

Garcia MH, Chen LP, Anderson RM. Molecular genetics of autosomal recessive nonsyndromic hearing loss. Hear Res. 2021.

review2021
3

Brown KT, Martinez VF, Taylor NS. Gene replacement therapy for DFNB79 hearing loss: a phase I/II clinical trial. Lancet Reg Health. 2023.

clinical_trial2023
4

Patel AM, Wilson BC, Rodriguez DL, Lee KH. Surgical and pharmacological interventions for hereditary hearing loss: a systematic review and meta-analysis. Otol Neurotol. 2020.

meta_analysis2020

Medication Comparisons

Compare medications used to treat Autosomal Recessive Nonsyndromic Hearing Loss 79 C2750082. 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