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Autosomal Recessive Nonsyndromic Deafness 26
An autosomal recessive nonsyndromic deafness that is caused by homozygous mutation in the GAB1 gene on chromosome 4q31.
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
An autosomal recessive nonsyndromic deafness that is caused by homozygous mutation in the GAB1 gene on chromosome 4q31.
Resources
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Talk with people who understand, share what helps, and find support from others living with autosomal recessive nonsyndromic deafness 26. Private, moderated, and free.
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