Living with Autosomal dominant nonsyndromic hearing loss 22
An inherited form of hearing loss that is passed down in families.
Understanding Autosomal dominant nonsyndromic hearing loss 22
DFNA22 is a type of deafness that runs in families. GARD does not list other details such as when it starts or how it changes over time.
Signs & symptoms
GARD doesn't list specific symptoms for this condition yet, but hearing loss is the main feature.
- 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.
Care & treatment
- Care team
- A doctor familiar with rare conditions, plus specialists as needed
- Expert care
- Ask about multidisciplinary care centers for rare conditions
- 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 rare disease patient organizations for support
- 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 caused by a change in the MYO6 gene (myosin VI) on chromosome 6. A change in just one copy of the gene can lead to DFNA22.
Also known as: autosomal dominant nonsyndromic deafness 22; dfna 22; dfna22 nonsyndromic hearing loss and deafness
Patient organizations
Rare-disease groups that can help
- Global GenesRare Diseases · United States
- National Organization for Rare DisordersRare Diseases · United States
- Genetic AllianceRare Diseases · United States
- RARE FoundationRare Diseases · United States
You are more than your diagnosis
Perspectives from people navigating life with Autosomal dominant nonsyndromic hearing loss 22.
Explore research for Autosomal dominant nonsyndromic hearing loss 22
Explore actively recruiting Autosomal dominant nonsyndromic hearing loss 22 studies with HealthSpark.
Find actively recruiting studies for Autosomal dominant nonsyndromic hearing loss 22 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 dominant nonsyndromic hearing loss 22 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 dominant nonsyndromic hearing loss 22
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 dominant nonsyndromic hearing loss 22 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.