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What is Branchiootic syndrome 3?

What is Branchiootic syndrome 3?

  • Branchiootic syndrome 3: A rare inherited disorder characterized by branchial and ear abnormalities. The hearing loss is variable with respect to severity and age of onset. Type 3 is caused by a defect chromosome 14q23. It is similar to the branchio-oto-renal syndrome except it doesn't involve any kidney abnormalities.

Branchiootic syndrome 3: Introduction

Types of Branchiootic syndrome 3:

Broader types of Branchiootic syndrome 3:

What causes Branchiootic syndrome 3?

Causes of Branchiootic syndrome 3: see causes of Branchiootic syndrome 3

What are the symptoms of Branchiootic syndrome 3?

Symptoms of Branchiootic syndrome 3: see symptoms of Branchiootic syndrome 3

Branchiootic syndrome 3: Testing

Diagnostic testing: see tests for Branchiootic syndrome 3.

How is it treated?

Doctors and Medical Specialists for Branchiootic syndrome 3: Medical Geneticist ; see also doctors and medical specialists for Branchiootic syndrome 3.
Treatments for Branchiootic syndrome 3: see treatments for Branchiootic syndrome 3

Name and Aliases of Branchiootic syndrome 3

Main name of condition: Branchiootic syndrome 3

Other names or spellings for Branchiootic syndrome 3:

BOS3, BO syndrome 3

 

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