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Diseases » Connexin 26 anomaly » Summary

What is Connexin 26 anomaly?

What is Connexin 26 anomaly?

  • Connexin 26 anomaly: A genetic mutation that causes congenital deafness.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Connexin 26 anomaly as a "rare disease".
Source - Orphanet

Connexin 26 anomaly: Introduction

Types of Connexin 26 anomaly:

Broader types of Connexin 26 anomaly:

What causes Connexin 26 anomaly?

Causes of Connexin 26 anomaly: see causes of Connexin 26 anomaly

What are the symptoms of Connexin 26 anomaly?

Symptoms of Connexin 26 anomaly: see symptoms of Connexin 26 anomaly

Connexin 26 anomaly: Testing

Diagnostic testing: see tests for Connexin 26 anomaly.

How is it treated?

Doctors and Medical Specialists for Connexin 26 anomaly: Medical Geneticist ; see also doctors and medical specialists for Connexin 26 anomaly.
Treatments for Connexin 26 anomaly: see treatments for Connexin 26 anomaly

Name of Connexin 26 anomaly

Main name of condition: Connexin 26 anomaly


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