Living with Autosomal recessive nonsyndromic hearing loss 47
A rare inherited form of hearing loss with no other health problems.
Understanding Autosomal recessive nonsyndromic hearing loss 47
The hearing loss is linked to changes in a specific area on chromosome 2. A change in both copies of the gene is usually needed to have the condition.
Signs & symptoms
Symptoms vary from person to person. GARD lists this as the most common:
- Hearing loss
Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.
Diagnosis
- 1Talk with your doctor
Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.
- 2See a specialist
Your doctor may refer you to a specialist who knows rare conditions.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
- 4Connect with expert centers
Hearing Loss Association of America may keep lists of experts for this condition.
Care & treatment
- Care team
- A doctor familiar with rare conditions, plus specialists as needed
- Expert care
- Expert lists: Hearing Loss Association of America
- Treatment
- GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
- Research
- Clinical trials and observational studies may be options. See the research section below.
General information, not medical advice. Your care team makes the decisions.
Everyday life
Living with a rare condition is easier with support.
- Connect with Hearing Loss Association of America
- Keep notes on symptoms, changes and questions for appointments
- Ask about patient registries that help research
- Look into financial aid and travel resources for care visits
Quick facts
It is linked to changes in a specific area on chromosome 2. It is autosomal recessive, so a child inherits a changed copy of the gene from each parent.
Also known as: autosomal recessive nonsyndromic deafness 47; deafness, autosomal recessive 47; deafness, neurosensory, autosomal recessive 47
Patient organizations
- Hearing Loss Association of AmericaAutosomal recessive nonsyndromic hearing loss 47 · United States
You are more than your diagnosis
Perspectives from people navigating life with Autosomal recessive nonsyndromic hearing loss 47.
Explore research for Autosomal recessive nonsyndromic hearing loss 47
Explore actively recruiting Autosomal recessive nonsyndromic hearing loss 47 studies with HealthSpark.
Find actively recruiting studies for Autosomal recessive nonsyndromic hearing loss 47 with HealthSpark. Share your city to explore research near you.
- Recruiting studies from ClinicalTrials.gov
- Share your city to look for research near you
- Eligibility is confirmed by the study team
Powered by HealthSpark, our AI chat helper
I can help you find recruiting Autosomal recessive nonsyndromic hearing loss 47 studies. Enter a ZIP code, address or city below and I'll look within 50 miles.
Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.
Get Signals for Autosomal recessive nonsyndromic hearing loss 47
Stay in the loop with community stories and updates from medical researchers.
Create a living journal that talks back
HealthStory evolves private journaling with a living AI journal that talks back and asks thoughtful questions, helping you capture your Autosomal recessive nonsyndromic hearing loss 47 experiences more deeply and prepare for better conversations with your doctors and care team.
Your journal is private. Sharing your story publicly is a separate choice, made with Share your story above.