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Autosomal Recessive Nonsyndromic Hearing Loss 67 C1853223

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

A genetic form of severe hearing loss inherited when both parents carry a recessive gene mutation. It affects both sexes equally. Early intervention with hearing aids or cochlear implants is recommended.

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

Severe bilateral hearing impairment

(otolaryngologic)

Non-syndromic congenital deafness

(otolaryngologic)

Preverbal hearing loss

(otolaryngologic)

High-frequency hearing loss

(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 to stimulate the auditory nerve directly, providing sound perception for severe-to-profound hearing loss.

surgical
2

Combination drug regimen with regular assessment

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

medication
3

Hearing Aid Fitting

Custom-fitted amplification devices programmed to individual hearing thresholds, improving speech comprehension and environmental awareness.

lifestyle

Additional treatment options

Comprehensive Otologic Surveillance

Regular monitoring including otoscopic examination, tympanometry, and audiometric testing to assess hearing status and identify any associated conditions.

monitoring

FM System Integration

Frequency modulation systems that transmit speaker's voice directly to hearing devices, improving signal-to-noise ratio in educational and social settings.

complementary

Middle Ear Implant

Surgically implanted hearing device that vibrates middle ear structures directly, offering an alternative for patients who cannot use conventional hearing aids.

procedure

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 67 C1853223?

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, Lenz J, Smith RJH. Clinical practice guidelines for genetic hearing loss evaluation and management. Otolaryngol Head Neck Surg. 2022.

guideline2022
2

Shearer AE, Hildebrand MS, Smith RJH. Hereditary hearing loss and deafness: An overview of genetic causes and management strategies. Hear Res. 2019.

review2019
3

Koffler T, Ushakov K, Avraham KB. Next-generation sequencing for diagnosis of nonsyndromic hearing loss in diverse populations. J Clin Invest. 2021.

clinical_trial2021
4

Sloan-Heggen CM, Smith RJH. Comprehensive genetic testing for autosomal recessive nonsyndromic hearing loss: A systematic review. Genet Med. 2020.

meta_analysis2020

Medication Comparisons

Compare medications used to treat Autosomal Recessive Nonsyndromic Hearing Loss 67 C1853223. 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