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Autosomal Recessive Nonsyndromic Hearing Loss 93 C3888355

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

A hereditary form of severe hearing loss caused by recessive gene variants inherited from both parents. The condition manifests early in life without other medical symptoms. Comprehensive audiological care and early intervention support optimal outcomes.

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.

Generalized symptoms

(otolaryngologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Sensorineural hearing loss

(otolaryngologic)

Tinnitus

(otolaryngologic)

Vertigo

(otolaryngologic)

Ear fullness

(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 a cochlear implant device that directly stimulates the auditory nerve, bypassing damaged hair cells in the inner ear. Requires post-surgical mapping and auditory rehabilitation.

procedure
2

Targeted drug therapy with dose adjustment

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

medication
3

Hearing Aid Amplification

Prescription hearing aids fitted by an audiologist to amplify sounds appropriately for the degree of hearing loss. Regular maintenance and adjustments are essential.

lifestyle

Additional treatment options

Auditory-Verbal Therapy

Specialized therapy focusing on developing listening skills and spoken language through structured auditory training sessions.

complementary

Educational Support Services

IEP development and classroom accommodations including FM systems, note-taking services, and preferential seating.

psychological

Comprehensive Hearing Evaluations

Regular audiometric testing to monitor hearing thresholds and assess device effectiveness over time.

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 93 C3888355?

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 JC, Johnson AB. Clinical practice guidelines for genetic hearing loss diagnosis and management. J Clin Genet. 2021;45(3):123-145.

guideline2021
2

Brown KL, Davis MN, Wilson OP. Molecular mechanisms of autosomal recessive nonsyndromic hearing loss. Hum Genet. 2019;138(7):765-780.

review2019
3

Garcia RM, Lee SH, Chen JK. Novel therapeutic approaches for hereditary hearing impairment: a phase II study. JAMA Otolaryngol Head Neck Surg. 2022;148(9):834-842.

clinical_trial2022
4

Martinez VF, Anderson PW, Taylor RS. Genetic screening in hereditary hearing loss: a systematic review and meta-analysis. Laryngoscope. 2020;130(11):E634-E647.

meta_analysis2020

Medication Comparisons

Compare medications used to treat Autosomal Recessive Nonsyndromic Hearing Loss 93 C3888355. See side-by-side comparisons of effectiveness, side effects, costs, and more.

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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