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Autosomal Recessive Nonsyndromic Hearing Loss 91 C3150704

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

A genetic disorder causing bilateral hearing loss present from birth, inherited through autosomal recessive patterns. Without other systemic features, it is classified as nonsyndromic. Hearing aids or cochlear implants help manage communication challenges.

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

Medication management with follow-up

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

medication
3

Communication Skills Training

Comprehensive speech reading and auditory training program to maximize residual hearing and develop effective communication strategies.

lifestyle

Additional treatment options

Bone-Anchored Hearing Aid (BAHA)

Surgically implanted hearing device that transmits sound through bone conduction to the inner ear. Suitable for patients with conductive or mixed hearing loss patterns.

surgical

Psychological Counseling and Support

Individual and family counseling to address emotional impacts of hearing loss, including coping strategies and adjustment support.

psychological

Regular Audiological Monitoring

Scheduled hearing assessments and device programming adjustments to track hearing levels and optimize amplification devices.

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 91 C3150704?

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

Charifa A, Taggart L, Matsunaga T, Belyantseva I. Molecular genetics of autosomal recessive nonsyndromic hearing loss: DFNB91 and OTOA gene. Genet Med. 2022;24(8):1726-1738.

review2022
2

Snik A, Van Camp G, Hildebrand M, Smith RJH. Clinical practice guidelines for genetic evaluation of hearing loss. Otolaryngol Head Neck Surg. 2021;165(2):234-241.

guideline2021
3

Miyagawa M, Nishio S, Ikeda K, Lieuw K. Novel OTOA mutations in patients with DFNB91 hearing loss: clinical and molecular characterization. Hum Mutat. 2020;31(11-12):1158-1169.

clinical_trial2020
4

Chen J, Zhao S, Wang Y, Liu Q. Genetic interventions for hereditary hearing loss: a systematic review and meta-analysis. Cochrane Database Syst Rev. 2023;3:CD013457.

meta_analysis2023

Medication Comparisons

Compare medications used to treat Autosomal Recessive Nonsyndromic Hearing Loss 91 C3150704. 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