Autosomal Recessive Nonsyndromic Hearing Loss 66 C1857750
A genetic hearing loss condition caused by autosomal recessive inheritance. Both parents typically carry one mutated copy without being affected. Hearing amplification devices or implants can assist communication.
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.
Early-onset bilateral hearing loss
(otolaryngologic)Generalized symptoms
(otolaryngologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Sensorineural auditory deficit
(otolaryngologic)Cochlear hearing impairment
(otolaryngologic)Audiometric threshold elevation
(otolaryngologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
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
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.
Targeted drug therapy with dose adjustment
Active treatment with regular monitoring by a healthcare provider is recommended.
Hearing Aid Fitting
Custom-fitted amplification devices programmed to individual hearing thresholds, improving speech comprehension and environmental awareness.
Additional treatment options
Auditoryverbal Therapy
Specialized therapy focusing on developing listening skills and spoken language through structured auditory training and speech therapy sessions.
complementaryGenetic Counseling and Family Planning
Comprehensive genetic counseling to discuss inheritance patterns, recurrence risks, and prenatal testing options for affected families.
monitoringBone-Anchored Hearing System
Surgically implanted bone conduction device for cases with conductive or mixed hearing loss component, bypassing middle ear abnormalities.
procedureWhen 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.
What is Autosomal Recessive Nonsyndromic Hearing Loss 66 C1857750?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Shearer AE, Hildebrand MS, Sloan CM, Smith RJ. Deafness and Hereditary Hearing Loss Overview. GeneReviews. 2023.
Alford RL, Arnos KS, Fox M, et al. American College of Medical Genetics and Genomics guideline for the evaluation of children with sensorineural hearing loss. Genet Med. 2022.
Matsunaga T, Mutai H, Kondo Y, et al. Clinical and genetic study of autosomal recessive nonsyndromic hearing loss in Japanese population. Otolaryngol Head Neck Surg. 2019.
Sloan-Heggen CM, Bierer AO, Shearer AE, et al. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. Hum Genet. 2016.
Medication Comparisons
Compare medications used to treat Autosomal Recessive Nonsyndromic Hearing Loss 66 C1857750. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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