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Autosomal Recessive Nonsyndromic Deafness 107
An autosomal recessive nonsyndromic deafness that is caused by compound heterozygous mutation in the WBP2 gene on chromosome 17q25.
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 compound heterozygous mutation in the WBP2 gene on chromosome 17q25.
Resources
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