Community
Autosomal-Mitochondrial Sensorineural Deafness
A sensorineural hearing loss characterized by progressive, severe to profound deafness that is caused by digenic inheritance of mutations in the mitochondrial gene MTRNR1 and an unidentified nuclear gene.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
A sensorineural hearing loss characterized by progressive, severe to profound deafness that is caused by digenic inheritance of mutations in the mitochondrial gene MTRNR1 and an unidentified nuclear gene.
Resources
Join the Autosomal-Mitochondrial Sensorineural Deafness community
Talk with people who understand, share what helps, and find support from others living with autosomal-mitochondrial sensorineural deafness. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.