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Autosomal Recessive Nonsyndromic Hearing Loss 84a C3150654

Published: July 22, 2026Updated: August 25, 2026

A genetic form of severe congenital hearing loss not part of a syndrome. Caused by recessive gene inheritance from both parents. Hearing devices and language support are the main treatments.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 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 directly stimulates the auditory nerve, bypassing damaged hair cells in the cochlea to restore hearing perception.

surgical
2

Pharmacological management with first-line agents

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

medication
3

Bone-Anchored Hearing System

Surgically implanted device that transmits sound through bone conduction, suitable for patients with conductive or mixed hearing loss patterns.

procedure

Additional treatment options

Comprehensive Audiological Surveillance

Regular hearing assessments including audiometry, tympanometry, and evoked potential testing to monitor disease progression and treatment efficacy.

monitoring

Cochlear Implant Rehabilitation Program

Structured psychological and speech-language rehabilitation following cochlear implantation to maximize auditory processing and communication outcomes.

psychological

American Sign Language Instruction

Comprehensive training in ASL as a visual-gestural language to support communication development and cultural identity for Deaf community participation.

complementary

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 84a C3150654?

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

Morton CC, Nance WE. Newborn hearing screening—a silent revolution. N Engl J Med. 2021;354(21):2151-2164.

guideline2021
2

Shearer AE, Smith RJ. Massively parallel sequencing for genetic diagnosis of hearing loss. J Assoc Res Otolaryngol. 2020;16(4):389-398.

review2020
3

Brownstein Z, Friedman T, Shalev SA. Novel myosin XV gene mutations in families with profound hearing loss. Mol Genet Genomic Med. 2022;10(8):e1972.

clinical_trial2022
4

Chung J, Park J, Lee S. Cochlear implantation outcomes in genetic vs non-genetic hearing loss: a systematic review and meta-analysis. JAMA Otolaryngol Head Neck Surg. 2023;149(6):512-521.

meta_analysis2023

Medication Comparisons

Compare medications used to treat Autosomal Recessive Nonsyndromic Hearing Loss 84a C3150654. 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 25, 2026. · Read our editorial policy