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Autosomal Dominant Congenital Deafness with Onychodystrophy
A syndrome that is characterized by autosomal dominant inheritance of congenital deafness and onychodystrophy and that is caused by heterozygous mutation in the ATP6V1B2 gene on chromosome 8p21.
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.
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Overview
A syndrome that is characterized by autosomal dominant inheritance of congenital deafness and onychodystrophy and that is caused by heterozygous mutation in the ATP6V1B2 gene on chromosome 8p21.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.